Bioresorbable silicon electronics for transient implants

ABSTRACT

Provided are implantable and bioresorbable medical devices comprising a bioresorbable substrate and an electronic circuit supported by the bioresorbable substrate. The electronic circuit comprises a membrane of silicon having a thickness less than or equal to 5 μm and an array of dissolvable electrodes, wherein the dissolvable electrodes are formed from the membrane of silicon. The electronic circuit is configured to conformally contact a biological tissue and electrically interface with biological tissue during use. The silicon may be highly doped to provide the requisite characteristics for electrically interfacing with biological tissue, and may be further used to form other components of the electronic circuit, including back-plane transistors electrically connected to the electrode array.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority from U.S. Provisional Patent Application No. 62/254,118 filed Nov. 11, 2015, which is hereby incorporated by reference in its entirety to the extent not inconsistent herewith.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable.

BACKGROUND OF INVENTION

With the continued advance of high performance electronic systems formed from device-grade, monocrystalline silicon as the semiconductor foundation, the ability to reliably deploy implantable monitoring systems has correspondingly increased. One disadvantage of such implantable devices is the need to remove them from the patient to avoid unwanted side effects, including due to the risk of an unwanted immune response, infection or irritation. Accordingly, effort has been devoted to designing implants and related sensors that are bioresorbable. See, for example, PCT/US16/40717 (filed Jul. 1, 2016); U.S. patent application Ser. No. 15/146,629 (filed May 4, 2016); and U.S. Pat. No. 8,666,471.

The focused effort toward an implantable and bioresorbable medical device is because such devices advantageously avoids the need for a separate surgical procedure to remove the implanted device. Instead, the device simply can be dissolved and removed from the implant site by natural biological and chemical processes.

A concern with implantable and bioresorbable medical devices is the ability to reliably control dissolution of the device after implantation so that device functionality is maintained over a desired device lifetime. For example, electronic circuits may have particular locations vulnerable to failure in a biological environment. The failure may be unforeseen and unpredictable, with minor variations in operating conditions leading to potentially wide changes in device lifetime, particularly for bioresorbable metals. In contrast, there is a concern regarding devices that are overly engineered to maintain functionality at the expense of the ability to bioresorb over a desired timeframe to minimize or avoid unwanted complications. Provided herein are devices and related methods that address this need in the art.

SUMMARY OF THE INVENTION

Devices and related methods provided herein utilize a specially configured membrane of silicon to form active electrodes that reliably interface with tissue while having a well-controlled dissolution rate. In particular, a highly doped and thin silicon membrane is processed and patterned to form an array of electrodes that can dissolve when contacted with a biofluid and achieve the desired bioresorption characteristics, thereby avoiding the need for medical intervention to remove the implanted device. Conventional corresponding bioresorbable metals, in contrast, suffer from comparatively fast dissolution kinetics, with tendency for uncontrolled degradation arising from cracking, fragmentation and flaking during bioresorption. The thin silicon membrane utilized herein not only forms the basis of active materials that electrically interface with tissue for sensing or for stimulation, but also can be used for the backplane transistors to access high-speed multiplexed addressing of the electrodes. In this manner, the silicon membrane may be thin, such as less than 10 μm, or less than 5 μm, or less than 1 μm, thereby providing desired dissolution characteristics. Similarly, various other components of the device, including substrate, insulators, encapsulating layers, electrical interconnects, may also have a thin layout configuration to further facilitate controlled dissolution, bioresorption and device mechanical parameters, such as flexibility, bendability, stretchability and/or rigidity, for implantation to a tissue of interest. The device physical properties of stretchability, net flexural rigidity, and bending modulus, may be selected to match an underlying tissue of interest.

Provided herein are implantable and bioresorbable medical devices and methods related thereto. For example, the device may comprise a bioresorbable substrate; an electronic circuit supported by the bioresorbable substrate, wherein the electronic circuit comprises a membrane of silicon (“Si membrane”), such as a membrane having a thickness less than or equal to 10 μm or 5 μm, or a thickness less than or equal to 1 μm. To reflect the small thickness of the Si membrane, the Si membrane is also referred herein as a “nanomembrane.” The Si membrane may be processed and patterned to provide a desired circuit functionality and geometry, as described herein. For example, an array of dissolvable electrodes, including a multiplexed array, may be formed from the membrane of silicon. The electronic circuit is configured to conformally contact and electrically interface with a biological tissue, including detecting electrical activity of biological tissue during use. In this manner, the entire device may be similarly configured to ensure conformal contact is reliably achieved, including by selection of shape conformable components of the device, such as with thin and flexible bioresorbable substrates and additional elements of the electronic circuit, such as backplane transistors also formed from the Si membrane. The silicon membrane may be formed of thin films of amorphous, polycrystalline and single crystal semiconductor materials (e.g. polycrystalline silicon, amorphous silicon). The silicon membrane may comprise polycrystalline or single-crystalline silicon.

The dissolvable electrodes of any the systems provided herein may be configured to undergo hydrolysis upon contact with a biofluid.

The devices may also be described in terms of various additional circuit components to impart desired functionality and operating characteristics. For example, any of the devices may further comprise an array of backplane transistors formed from the membrane of silicon. The transistors may be in electrical contact with the array of dissolvable electrodes in order to achieve a desired high speed multiplexed addressing of the array of dissolvable electrodes. The transistors may be metal-oxide-semiconductor field-effect transistors (MOSFETs).

Examples of MOSFETs compatible with desired conformability and dissolution characteristics include those comprising a thin film of a metal, a gate dielectric and an interlayer dielectric. A MOSFET may include a metal layer comprising Mo having a thickness less than 500 nm; a gate dielectric comprising SiO₂ having a thickness less than 200 nm; and an interlayer dielectric comprising a multilayer stack of SiO₂ with a thickness less than 400 nm, Si₃N₄ with a thickness less than 500 nm, and SiO₂ with a thickness less than 400 nm.

Any of the devices may further comprise for each electrode: a buffer transistor electrically connected to the electrode for buffering of a measured tissue potential; and a multiplexing transistor electrically connected to the electrode for multiplexing of the array of electrodes.

To further facilitate multiplexed addressing and high-speed control and/or data acquisition, the devices may further comprise a second thin layer of metal to define column select lines electrically connected to the array of electrodes.

The membrane of silicon may be patterned to form a plurality of parallel silicon ribbons with an encapsulation layer having a plurality of passages that is aligned with the parallel silicon ribbons to form an array of exposed silicon corresponding to the active regions of the array of dissolvable electrodes electrically interconnected with regions of encapsulated silicon ribbons. In this manner, the electrodes may be electrically connected to external connectors, such as for connection to a power supply, controller, and/or wireless communicator.

Any of the devices may further comprise a plurality MOSFETs formed from the membrane of silicon, wherein the membrane of silicon serves as both an active semiconductor material and as a tissue interface electrode.

The devices may be described as having an active region at a distal end of the parallel silicon ribbons connected to external electrical connectors separated from the distal end by a longitudinal distance, such as a distance that is greater than or equal to 3 mm. “Active region” of the Si membrane refers to the portion of the electrode capable of electrically interfacing with biological tissue, specifically the unencapsulated and uninsulated portion that is exposed to the biological environment.

The electrodes may be configured for physical contact with underlying tissue and be in electrical contact with said backplane transistor through vertical interconnects. The vertical interconnects may comprise vias through which electronic signals pass, including through an electrical conductor positioned through the vias.

The devices may have one or more additional layers to achieve desired operating characteristics, depending on the application of interest. For example, encapsulation or barrier layers may be incorporated into the devices to achieve a desired operating lifetime and/or improve control or parameter measurement without sacrificing the ability to achieve the desired electrical interfacing.

Any of the devices may further comprise an encapsulation layer that covers the backplane transistors and the membrane of silicon. As desired, passages may be positioned to facilitate improved electrical contact with active electrode regions and underlying tissue. The encapsulation layer may have a thickness less than or equal to 2 μm. The encapsulation layer may comprise a trilayer of SiO₂/Si₃N₄/SiO₂. A plurality of passages may be positioned through the encapsulation layer and in spatial alignment with an active region of each of said electrodes. In this context, “spatial alignment” refers to the position of the passage or opening through the encapsulation layer such that reliable electrical contact between the active area of the electrode and the corresponding surface being measured is achieved. This may be further defined in a quantitative manner, wherein at least 80%, at least 90%, at least 99%, or all of the area of the active electrode has a vertical correspondence with an opening. Similarly, the passage opening area may have at least 80%, at least 90%, at least 99%, or all vertical correspondence to an underlying active electrode region. Accordingly, spatial alignment may also include entire correspondence between opening and active electrode region.

Any of the devices provided herein may also be described in terms of a device lifetime, such as a device configured for accurate measurement of a biological parameter over a device lifetime. Depending on the application of interest, the device is configured to have any of a wide range of device lifetimes. For example, a device lifetime for a chronic monitoring application may be greater than or equal to 10 days, such as lasting up to the order of 1 to 6 months. Alternatively, a device lifetime for an acute monitoring application may be less than or equal to 2 days. In this context, “accurate measurement” refers to a deviation from a measured value with a conventional system (e.g., non-dissolvable electrodes) that is less than 20%, less than 10%, or less than 5%. Accordingly, a bioresorption lifetime is generally longer than the device lifetime, reflecting that a portion of the device may still be observed at the implant site after the device is considered non-functional. For example, once the device lifetime has passed, it may take an additional day or week for the natural biochemical processes to result in no detectable portion of the device remaining at the implant site.

The membrane of silicon may have a thickness that decreases as a function of implant duration, wherein the device maintains functionality for a decrease in thickness of up to 70%. In this aspect, “functionality” refers to the ability for the device to reliably provide the desired functionality. For example, at least 80% of the electrodes in the array that are able to consistently measure electric potential and/or apply and electric potential at a value that is within at least 80% of desired.

The device lifetime may be controlled by a variety of physical parameter adjustments. For example, device lifetime may be increased with increasing dopant concentration and/or increasing Si membrane thickness.

The membrane of silicon may be doped with a high concentration of dopant. “High concentration” refers to an amount of dopant sufficient to provide desired functionality to the silicon membrane, including the ability to conduct charge for the electric potential sensing and/or electrical stimulation by the array of electrodes. The high concentration may also be described in quantitative amounts, such as greater than or equal to 5×10¹⁶/cm³ and less than or equal to 2×10²⁰/cm³, or greater than about 10¹⁸/cm³ and less than 2×10²⁰/cm³. As desired, any number of dopant materials may be used, including a dopant selected from the group consisting of phosphorus and boron.

The devices may further comprise an insulation layer and electrical interconnects that electrically connect the electrodes, wherein the insulation layer electrically isolates interconnects from biofluids and biological tissue during use.

The insulation layer may comprise a layer of SiO₂ having a thickness less than or equal to 200 nm.

The membrane of silicon may further comprise terminal pads configured to electrically interface with a biological tissue. The terminal pads may correspond to exposed Si of membrane of Si. Other portions of the Si of membrane may be covered by an insulation layer.

Any of the devices provided herein may be configured to undergo bioresorption at least partially by controlled dissolution, including controlled dissolution of the membrane of Si. The controlled dissolution may be characterized by one or more of no observable: cracks, flakes, particulates, or decrease in surface smoothness over the time course of functional device lifetime. “No observable” may alternatively be expressed in quantitative terms, including less than 5% or less than 1% compared to an initial state of the material. In this manner, the bioresorption is relatively uniform and steady, and avoids cracking, flaking, particulate release and pitting associated with a rapid and sudden onset of device breakdown, including for electrodes formed of metal.

The controlled dissolution may be described as having an average dissolution rate characterized by a decrease in Si membrane thickness that is greater than or equal to 5 nm/day and less than or equal to 15 nm/day.

The dissolution rate for other non-Si membrane components of the device, including an insulating layer and/or substrate, may be between 3 nm/day and 12 nm/day.

The device may have one or more material parameters selected to obtain a desired dissolution time of the device, the material parameters including one or more of thickness, doping level, composition of polymer substrate.

The device may also be characterized in terms of biocompatibility during use, such as during use there is no detectable long-term adverse immune response.

The device may also be characterized in terms of its conformability, such as being capable of being bent from a planar configuration to a curved configuration with a radius of curvature up to 3 mm without adverse degradation of device functionality. In this context, “adverse degradation” may be defined in terms of deviation of a measured parameter, such as a deviation that is less than or equal to 20%, 10% or 5%, compared to the measure parameter in the planar configuration.

Any of the devices provided herein may be used for spatio-temporal mapping of electrical activity for a biological tissue, such as of the brain, including the cerebral cortex of brain.

Also provided herein are methods of electrically interfacing with biological tissue using any of the devices described herein. For example, the method may comprising the steps of: implanting an implantable and bioresorbable medical device described herein adjacent to a biological tissue; electrically interfacing the device with the biological tissue, wherein the interfacing is one or more of: electrically stimulating or electrically monitoring; and maintaining device functionality over a device lifetime; and dissolving the device so that after the device lifetime no detectable device remains at the implant site. The device lifetime may be selected for the application of interest, including short-term, acute to long-term chronic. After the desired device lifetime, sufficient dissolution has occurred that the device no longer reliably functions, including for example a 70% or greater dissolution of Si membrane thickness.

Also provided herein are methods of making any of the devices described herein.

Without wishing to be bound by any particular theory, there may be discussion herein of beliefs or understandings of underlying principles relating to the devices and methods disclosed herein. It is recognized that regardless of the ultimate correctness of any mechanistic explanation or hypothesis, an embodiment of the invention can nonetheless be operative and useful.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A-1G. Thin, flexible neural electrode arrays with fully bioresorbable construction based on patterned silicon nanomembranes (Si NMs) as the conducting component. FIG. 1A: Schematic exploded view illustration of the construction of a passive, bioresorbable neural electrode arrays for ECoG and subdermal EEG measurements. A photolithographically patterned, n-doped Si NMs (˜300 nm thick) defines the electrodes and interconnects. A film of SiO₂ (˜100 nm thick) and a foil of PLGA (˜30 μm thick) serves as a bioresorbable encapsulating layer and substrate, respectively. The device connects to an external data acquisition (DAQ) system through an anisotropic conductive film interfaced to the Si NMs interconnects at contact pads at the edge. A magnified optical image of electrodes on the right highlights the sensing (Si NMs) and insulating (SiO₂) regions. FIG. 1B: Photographs of bioresorbable neural electrode arrays with 4 channels (top) and 256 (16×16 configuration) channels (bottom). FIG. 1C: Microscope image of a device on a hydrogel substrate immersed in an aqueous buffer solution (pH 7.4) at 37° C. FIG. 1D: Electrochemical impedance spectra measured at four different recording sites in an array configured for ECoG. FIG. 1E: Dissolution kinetics for phosphorus and boron doped Si NMs (˜300 nm thick, dopant concentration 10²⁰/cm³) during immersion in artificial cerebrospinal fluid (aCSF) pH 7.4 at 37° C. FIG. 1F: Distribution of principal strains extracted from finite-element modeling (FEM) of a device bent to a radius of curvature of 1 mm (center) and corresponding displacement profile (left) and image of an array wrapped around a cylindrical tube with a radius of 2 mm (right). FIG. 1G: Images collected at several stages of accelerated dissolution induced by immersion in an aqueous buffer solution (pH 10) at 37° C.

FIG. 2A-2G. In vivo neural recordings in rats using a passive, bioresorbable electrode array. The data presented here are representative of three separate acute experiments, each with a duration of ˜5-6 hours. FIG. 2A: Photograph of four-channel bioresorbable electrode array placed on the cortical surface of the left hemisphere of a rat. FIG. 2B: Sleep spindles recoded by a bioresorbable electrode and a nearby commercial stainless steel microwire electrode, as a control placed at 0.5 mm depth from the cortical surface. FIG. 2C: Interictal spiking activity captured by the bioresorbable electrode and the control electrode after topical application of bicuculine methodide. Both electrodes interface with the same hemisphere. Data were processed through a 0.1 Hz-5 kHz bandpass filter. Recordings by the bioresorbable electrode and the control electrode show consistent interictal spikes. FIG. 2D: Interictal spiking activity recorded by the bioresorbable electrode and the control electrode 30 minutes after topical application of bicuculine methodide. Both recordings exhibit high signal-to-noise ratio (Si: 42, Control electrodes: 32) for detecting epileptiform activity. FIG. 2E: Cartoon illustration of a bioresorbable array placed on the periosteum for subdermal EEG recordings. FIG. 2F: Theta oscillations and fast spindle-like oscillations recorded subdermally using bioresorbable electrodes during isoflurane anesthesia. FIG. 2G: Power density spectra of the theta oscillations recorded over a 5 min time window. The spectrum shows a clear peak at the expected frequency range.

FIG. 3A-3G. In vivo chronic recordings in rats using a passive, bioresorbable electrode array. The data presented here is representative of chronic recording experiments with a duration of 30 days. FIG. 3A: Photograph of a four-channel bioresorbable electrode array implanted on left hemisphere of the brain of a rat, for chronic recordings, with a coating gelfoam and a layer of dental cement. The array connects to a custom-built circular interface board through a flexible ACF cable. The inset shows the array and craniaotomy after application of a first layer of dental cement. FIG. 3B-3F: Representative ECoG signals recorded by the bioresorbable array and the control electrode on day 1, 8, 15, 30 and 33. Recordings from three electrodes from the bioresorbable array exhibit large scale oscillatory behavior consistent with small local and temporal variations. After functional dissolution (Day 33), signals from the bioresorbable array show no ECoG activity while the control electrode continues to show expected cortical potentials. FIG. 3G: High voltage rhythmic spikes observed during absence-like seizure activity recorded chronically.

FIG. 4A-4B. Immunohistology analysis. Double labeling for astrocytic marker GFAP (green) and microglia/macrophages marker Iba-1 (red) demonstrates moderate subpial gliosis at the implantation sites of both control (FIG. 4A, upper left panels) and bioresorbable (FIG. 4B, upper right panels) electrodes and a marked increase in the densities of activated round microglial cells, exclusively underneath the control electrodes (middle left panels). Cell nuclei are visualized with DAPI stain (blue). Scale bars represent 30 μm.

FIG. 5A-5E. Bioresorbable actively multiplexed neural electrode array. FIG. 5A: Schematic exploded view illustration of an actively multiplexed sensing system for high resolution ECoG, in a fully bioresorbable construction. This 8×8 embodiment includes 128 metal-oxide-semiconductor field-effect transistors (MOSFETs) where Si NMs serve as both the active semiconductor material and the neural interface electrodes. The metallization, the gate dielectric and the interlayer dielectric rely on thin films of Mo (˜300 nm thick) and SiO₂ (˜100 nm thick) and trilayers of SiO₂ (˜300 nm thick)/Si₃N₄ (˜400 nm thick)/SiO₂ (˜300 nm thick), respectively. A second layer of Mo (˜300 nm thick) defines column interface lines. A similar trilayer serves as the encapsulation. A film of poly(lactide-co-glycolide) (PLGA, ˜30 μm thick) forms the substrate. FIG. 5B: Optical micrograph images of a pair of unit cells at various stages of fabrication (left) and a picture of a complete system (right). FIG. 5C: The left frame shows linear (red) and log scale (blue) transfer curves for a representative n-channel MOSFET, for V_(g) swept from −5 to +5 V. The channel length (L_(ch)), and width (W) are 15 μm and 80 μm, respectively. The threshold voltage, mobility and on/off ratio are ˜1 V, ˜400 cm²/V·s and ˜10⁸, respectively, with Mo for source, drain and gate electrodes, and SiO₂ for gate dielectrics. The right frame shows current-voltage characteristics, for V_(g) from 0 to 2.5 V with 0.5 V steps. FIG. 5D: Output response of a unit cell with respect to an input sine wave (200 mV peak to peak) upon insertion in aqueous phosphate buffer solution (PBS, pH 7.4) at room temperature. FIG. 5E: Images collected at several stages of accelerated dissolution of a system immersed into an aqueous buffer solution (pH 12) at 37° C.

FIG. 6A-6G. Acute in vivo microscale electrocortigoraphy (μECoG) with a 64-channel, bioresorbable, actively multiplexed array of measurement electrodes. FIG. 6A: Data recorded from picrotoxin-induced spikes (clockwise spiral, lower-right to upper-left diagonal, upper-left to lower-right diagonal, and right-to-left sweep). The results correspond to measurements across the 64 channels of the array, and the average response (grey) from all channels. The waveforms are color-coded according to the relative latency of the spike maximum (blue is earliest, red is latest). FIG. 6B: Movie frames corresponding to each spike pattern, showing the varied spatial-temporal μECoG voltage patterns from all 64 electrodes at the labeled time. Blue indicates negative, and dark red indicates the highest peak-to-peak voltage observed for each electrode site. The frame interval and color scale are provided for each set of eight movie frames. FIG. 6C: Relative delay map for the band-pass filtered data of each spike activity from frame b, illustrating a clear phase singularity indicated by arrow. FIG. 6D: Illustration of the whisker stimulation locations (Stim. loc.: B1 and Stim. loc.: E3) in a rat model. FIG. 6E: Illustration of the barrel cortex and estimated relative location of the recording array based on evoked potential results. Visibly-activated whiskers indicated by color corresponding to the stimulation location. M=medial, C=caudal. FIG. 6F: Temporal characteristics of the potentials evoked by stimulation location 1 (left) and 2 (right). FIG. 6G: Spatial distribution of the potentials evoked by stimulation location 1 and 2. The color map indicates the evoked potential size, interpolated across the array.

FIG. 7A-7B. Materials and procedures for fabricating bioresorbable passive electrodes on biodegradable substrates (PLGA) and a device image. FIG. 7A: Schematic illustrations of key processes for fabricating bioresorbable passive electrodes: (1) printing highly n-doped Si on temporary substrates, (2) defining the mesh structure, followed etching by RIE and immersion buffered oxide etchant (BOE), (3) retrieving the device onto a PDMS slab, (4) printing the device onto a bioresorbable substrate (PLGA), and (5) removing the top D-PI layer. FIG. 7B: Optical image of a complete device.

FIG. 8. A photograph of a bioresorbable passive electrode array with a penny.

FIG. 9A-9C. EIS characterization of Si and Au. FIG. 9A: Schematic description of the equivalent circuit model used to fit EIS measurement results. C_(PE) is the constant phase element representing the double-layer capacitance; R_(CT) is the charge transfer resistance; and R_(S) is the solution resistance. FIG. 9B: Results of measurement (solid lines) and fitting (dashed lines) for the impedance. FIG. 9C: Representative values of C_(PE) and R_(CT) for Au and Si.

FIG. 10. Impedance spectra of phosphorus doped Si NM electrodes with different doping concentrations (10¹⁷/cm³, 10¹⁹/cm³, 10²⁰/cm³).

FIG. 11. Impedance spectra of boron and phosphorus doped Si NM electrodes with the same doping concentrations (10²⁰/cm³) for both boron and phosphorus.

FIG. 12. Impedance spectra of different thicknesses (300 nm, 210 nm, 120 nm) of sites of Si.

FIG. 13. Impedance spectra of phosphorus doped Si NM electrodes with the different areas (200×200 μm² (A1), 300×300 μm² (A2), 400×400 μm² (A3), 500×500 μm² (A4)) of sites.

FIG. 14. Hydrolysis kinetics for SiO₂ and Si₃N₄ used in the devices. Thicknesses as a function of time during dissolution in artificial cerebrospinal fluid (ACSF) at 37° C. The initial thicknesses were 300 nm for both SiO₂ and Si₃N₄.

FIG. 15. Impedance spectra of before and after bending with 2 mm bending radius of a bioresorbable passive electrode array.

FIG. 16A-16B. In vivo neural recordings in rats. FIG. 16A: Slow wave activity and FIG. 16B: k-complexes recorded using a bioresorbable electrode array and a control stainless steel microwire electrode.

FIG. 17. A photograph of bioresorbable passive electrode array placed onto the periosteum of a rat.

FIG. 18. Photographs of surgery associated with chronic recording experiments. Implanting the bioresorbable electrode arrays on a rat brain, applying the dental cement, and then burying the head stage board.

FIG. 19. Representative ECoG signals recorded by the bioresorbable array (Ch1, Ch2, and Ch3) and the control electrode on day 32.

FIG. 20. A photograph after the surgery of the device implantation, showing freely moving rat with a head stage connector.

FIG. 21. Clinical platinum electrodes for ECoG, 8×8 Electrode Grid (left), and 1×8 Strip Electrode (right).

FIG. 22. Schematic circuit diagram of a single unit cell containing two matched n-MOS transistors in an actively multiplexed, bioresorbable electrode array.

FIG. 23. Schematic illustration of a 8×8 array of actively multiplexed channels, showing the entire device (left), and the unit cell design (right).

FIG. 24. Schematic circuit diagram for an active shielding circuit for the actively multiplexed array.

FIG. 25. In vitro test setup for actively multiplexed array.

FIG. 26. Color map illustrating the spatial distribution of the electrode response, demonstrating the spatial uniformity of the gain of an actively multiplexed, bioresorbable electrode array and leakage current over time.

FIG. 27. Photograph of an implanted 8×8 actively multiplexed array (left hemisphere of rat brain) and a control electrode (right hemisphere of rat brain).

FIG. 28. Representative RMS power image maps from four different spike clusters (clockwise spiral, lower-right to upper-left diagonal, upper-left to lower-right diagonal, right-to-left sweep) illustrate the high sensitivity of the electrode array and the spatially localized nature of spikes.

DETAILED DESCRIPTION OF THE INVENTION

In general, the terms and phrases used herein have their art-recognized meaning, which can be found by reference to standard texts, journal references and contexts known to those skilled in the art. The following definitions are provided to clarify their specific use in the context of the invention.

“Spatio-temporally” or “spatio-temporal” refers to a parameter having a spatial pattern which may change over time. For example, electric potential over the brain surface changes with time, with different regions of the brain generating or propagating an electric potential under various conditions. A sleeping patient will have a different spatio-temporal waveform than an active person. A patient having a brain-generated seizure has a different spatio-temporal waveform than a patient not seizing. Accordingly, “spatio-temporally electrically interfacing” refers to spatial and temporal electrical connection between a device and a brain tissue, so that the spatio-temporal monitoring and/or actuation of the brain can occur.

“Electrically interfacing” refers to the ability to monitor and/or generate electrical potential with a biological tissue. The array and multiplex configuration allows for spatio-temporal monitoring and/or intervention with an applied electric field over a surface area. For example, electrical waveforms may be detected and/or applied, including for a detected waveform indicative of an adverse situation, depending on the tissue of interest. For brain, the adverse situation may be onset of a seizure. For heart, the adverse situation may be indicative of onset of a heart attack or failure. Of course, the devices are compatible with more passive monitoring and related transmission of data, including in real-time, for assessment and action by medical personnel.

“Brain tissue” refers to brain in the in vivo, in vitro, or the ex vitro environment. The brain may be from a human or a non-human, such as an animal.

“Conformable” refers to a device, material or substrate which has a bending stiffness sufficiently low to allow the device, material or substrate to adopt a desired contour profile, for example a contour profile allowing for conformal contact with a surface having a pattern of relief or recessed features. In certain embodiments, a desired contour profile is that of a tissue in a biological environment, for example heart tissue. “Deformable” is used similarly to conformable, and refers to a device, material or substrate can flex, bend, or conform without undue induced strain during deformation, specifically an induced strain below that required to induce mechanical fracture or permanent fatigue. In particular, the element is considered deformable if any induced stress associated with deformation is below the ultimate tensile stress or the yield stress.

“Electrical communication” or contact refers to an arrangement of two components of a device wherein electrical signal (e.g., current, potential) is passed between the two components. For example, each electrode in the array may be electrically connected to a pair of transistors, and the transistors may be connected to a current source or sink, and specifically, to a controller. The parts of the device that convey the electrical signal between the electrical components are herein referred to as “interconnects”.

A “component” is used broadly to refer to a material or individual component used in a device. An “interconnect” is one example of a component and refers to an electrically conducting material capable of establishing an electrical connection with a component or between components. In particular, an interconnect may establish electrical contact between components that are separate and/or can move with respect to each other. Depending on the desired device specifications, operation, and application, an interconnect is made from a suitable material. For applications where a high conductivity is required, typical interconnect metals may be used, including but not limited to copper, silver, gold, aluminum and the like, and alloys. Suitable conductive materials further include semiconductors, such as silicon and GaAs and other conducting materials such as indium tin oxide.

An interconnect that is “stretchable” or “flexible” is used herein to broadly refer to an interconnect capable of undergoing a variety of forces and strains such as stretching, bending and/or compression in one or more directions without adversely impacting electrical connection to, or electrical conduction from, a device component. Accordingly, a stretchable interconnect may be formed of a relatively brittle material, such as GaAs, yet remain capable of continued function even when exposed to a significant deformatory force (e.g., stretching, bending, compression) due to the interconnect's geometrical configuration. In an exemplary embodiment, a stretchable interconnect may undergo strain larger than 1%, optionally 10% or optionally 30% or optionally up to 100% without fracturing. In an example, the strain is generated by stretching an underlying elastomeric substrate to which at least a portion of the interconnect is bonded. For certain embodiments, flexible or stretchable interconnects include interconnects having wavy, meandering or serpentine shapes.

“Bending stiffness” is a mechanical property of a material, device or layer describing the resistance of the material, device or layer to an applied bending moment. Generally, bending stiffness is defined as the product of the modulus and area moment of inertia of the material, device or layer. A material having an inhomogeneous bending stiffness may optionally be described in terms of a “bulk” or “average” bending stiffness for the entire layer of material. A material made up of a plurality of components, e.g., substrate and barrier layers, electrical circuit, may be described in terms of a “net bending stiffness”, which is a compilation and average of each component's bending stiffness.

“Conformal contact” refers to contact established between a device and a receiving surface, which may for example be a target tissue in a biological environment. In one aspect, conformal contact involves a macroscopic adaptation of one or more surfaces (e.g., contact surfaces) of an implantable device to the overall shape of a tissue surface. In another aspect, conformal contact involves a microscopic adaptation of one or more surfaces (e.g., contact surfaces) of an implantable device to a tissue surface resulting in an intimate contact substantially free of voids. In an embodiment, conformal contact involves adaptation of a contact surface(s) of the implantable device to a receiving surface(s) of a tissue such that intimate contact is achieved, for example, wherein less than 20% of the surface area of a contact surface of the implantable device does not physically contact the receiving surface, or optionally less than 10% of a contact surface of the implantable device does not physically contact the receiving surface, or optionally less than 5% of a contact surface of the implantable device does not physically contact the receiving surface. Conformal contact includes large area conformal contact, for example, wherein conformal contact between a tissue and device component is over an area greater than or equal to 1000 mm², and optionally greater than or equal to 10,000 mm². In an aspect, the tissue is brain tissue. Conformal contact may also be described in terms of the maximum separation distance between the device and the underlying brain tissue that the device is interfaced with, such as a distance that is less than or equal to 1 mm. In addition, the tissue may have an intervening thin film of brain fluid between the brain tissue and the device. Accordingly, physical contact with brain tissue includes physical contact between the device and any biological film, including brain fluid, surrounding the brain, so long as electrical contact between the device and brain is maintained.

“Encapsulate” refers to the orientation of one structure such that it is at least partially, and in some cases completely, surrounded by one or more other structures, such as a substrate, adhesive layer or encapsulating layer. “Partially encapsulated” refers to the orientation of one structure such that it is partially surrounded by one or more other structures, for example, wherein 30%, or optionally 50% or optionally 90%, of the external surfaces of the structure is surrounded by one or more structures. “Completely encapsulated” refers to the orientation of one structure such that it is completely surrounded by one or more other structures. Devices may have partially or completely encapsulated inorganic semiconductor components, metallic conductor components and/or dielectric components, for example, via incorporation a polymer encapsulant, such as biopolymer, silk, a silk composite, or an elastomer encapsulant. The encapsulation may correspond to a substrate that supports an electronic device and a superstrate that covers the electronic device.

“Barrier layer” refers to a component spatially separating two or more other components or spatially separating a component from a structure, material, fluid or environment external to the device. In one embodiment, a barrier layer encapsulates one or more components. In some embodiments, a barrier layer separates one or more components from an aqueous solution, a biological tissue or both. The invention includes devices having one or more barrier layers, for example, one or more barrier layers positioned at the interface of the device with an external environment.

Devices and methods provided herein are useful for “monitoring” or “actuating” electrical spatio-temporal waveforms over the brain surface. Monitoring refers to measuring, and optionally encoding, spatio-temporal electrical waveform on the brain surface. Actuating refers to the electrodes of the device interacting with, stimulating, controlling, or otherwise affecting brain tissue, or a material (e.g., skull, skin) or fluid (e.g., cerebral fluid) in electrical contact therewith.

“Temporally adjacent time points” is a measure of the time resolution of the device. The ability to electrically detect changes in electrical potential in a brain location is constrained by how often the electrical measurement is made or the delay time between measurements. The ability to stimulate brain waveform change is similarly constrained.

“Electrical waveform” refers to a pattern of electric potential over the brain surface. A single waveform snapshot provides only limited information about the waveform at one single instance in time. Accordingly, a spatio-temporal profile requires monitoring of the waveform over a period of time. This provides information about the direction of travel of the waveform, how it initiates, propagates and terminates. That information is required to further identify a waveform as “abnormal” or “normal”.

The terms “flexible” and “bendable” are used synonymously in the present description and refer to the ability of a material, structure, device or device component to be deformed into a curved or bent shape without undergoing a transformation that introduces significant strain, such as strain characterizing the failure point of a material, structure, device or device component. In an exemplary embodiment, a flexible material, structure, device or device component may be deformed into a curved shape without introducing strain larger than or equal to 5%, for some applications larger than or equal to 1%, and for yet other applications larger than or equal to 0.5% in strain-sensitive regions. A used herein, some, but not necessarily all, flexible structures are also stretchable. A variety of properties provide flexible structures (e.g., device components) of the invention, including materials properties such as a low modulus, bending stiffness and flexural rigidity; physical dimensions such as small average thickness (e.g., less than 100 microns, optionally less than 10 microns and optionally less than 1 micron) and device geometries such as thin film and mesh geometries.

“Stretchable” refers to the ability of a material, structure, device or device component to be strained without undergoing fracture. In an exemplary embodiment, a stretchable material, structure, device or device component may undergo strain larger than 0.5% without fracturing, for some applications strain larger than 1% without fracturing and for yet other applications strain larger than 3% without fracturing. A used herein, many stretchable structures are also flexible. Some stretchable structures (e.g., device components) are engineered to be able to undergo compression, elongation and/or twisting so as to be able to deform without fracturing. Stretchable structures include thin film structures comprising stretchable materials, such as elastomers; bent structures capable of elongation, compression and/or twisting motion; and structures having an island-bridge geometry. Stretchable device components include structures having stretchable interconnects, such as stretchable electrical interconnects.

“Semiconductor” refers to any material that is an insulator at a low temperature, but which has an appreciable electrical conductivity at a temperatures of about 300 Kelvin. In the present description, use of the term semiconductor is intended to be consistent with use of this term in the art of microelectronics and electronic devices. Useful semiconductors include those comprising element semiconductors, such as silicon, germanium and diamond, and compound semiconductors, such as group IV compound semiconductors such as SiC and SiGe, group III-V semiconductors such as AlSb, AlAs, Aln, AlP, BN, GaSb, GaAs, GaN, GaP, InSb, InAs, InN, and InP, group III-V ternary semiconductors alloys such as Al_(x)Ga_(1-x)As, group II-VI semiconductors such as CsSe, CdS, CdTe, ZnO, ZnSe, ZnS, and ZnTe, group I-VII semiconductors CuCl, group IV-VI semiconductors such as PbS, PbTe and SnS, layer semiconductors such as PbI₂, MoS₂ and GaSe, oxide semiconductors such as CuO and Cu₂O. The term semiconductor includes intrinsic semiconductors and extrinsic semiconductors that are doped with one or more selected materials, including semiconductor having p-type doping materials and n-type doping materials, to provide beneficial electronic properties useful for a given application or device. The term semiconductor includes composite materials comprising a mixture of semiconductors and/or dopants. Specific semiconductor materials useful for in some embodiments include, but are not limited to, Si, Ge, SiC, AlP, AlAs, AlSb, GaN, GaP, GaAs, GaSb, InP, InAs, GaSb, InP, InAs, InSb, ZnO, ZnSe, ZnTe, CdS, CdSe, ZnSe, ZnTe, CdS, CdSe, CdTe, HgS, PbS, PbSe, PbTe, AlGaAs, AlInAs, AlInP, GaAsP, GalnAs, GaInP, AlGaAsSb, AlGaInP, and GalnAsP. Porous silicon semiconductor materials are useful for applications of aspects described herein in the field of sensors and light emitting materials, such as light emitting diodes (LEDs) and solid state lasers. Impurities of semiconductor materials are atoms, elements, ions and/or molecules other than the semiconductor material(s) themselves or any dopants provided to the semiconductor material. Impurities are undesirable materials present in semiconductor materials which may negatively impact the electronic properties of semiconductor materials, and include but are not limited to oxygen, carbon, and metals including heavy metals. Heavy metal impurities include, but are not limited to, the group of elements between copper and lead on the periodic table, calcium, sodium, and all ions, compounds and/or complexes thereof.

“Semiconductor element”, “semiconductor structure” and “semiconductor circuit element” are used synonymously in the present description and broadly refer to any semiconductor material, composition or structure, and expressly includes high quality single crystalline and polycrystalline semiconductors, semiconductor materials fabricated via high temperature processing, doped semiconductor materials, organic and inorganic semiconductors and composite semiconductor materials and structures having one or more additional semiconductor components and/or non-semiconductor components, such as dielectric layers or materials, electrodes and/or conducting layers or materials.

“Active circuit” and “active circuitry” refers to one or more device components configured for performing a specific function. Useful active circuits include, but are not limited to, amplifier circuits, multiplexing circuits, logic circuits, CMOS circuits, processors, and current limiting circuits. Useful active circuit elements include, but are not limited to, transistor elements and diode elements.

“Electrical contact” refers to the ability of two or more materials and/or structures that are capable of transferring charge between them, such as in the form of the transfer of electrons or ions. Electrical communication refers to a configuration of two or more components such that an electronic signal or charge carrier can be directly or indirectly transferred from one component to another. As used herein, electrical communication includes one way and two way electrical communication. In some embodiments, components in electrical communication are in direct electrical communication wherein an electronic signal or charge carrier is directly transferred from one component to another. In some embodiments, components in electrical communication are in indirect electrical communication wherein an electronic signal or charge carrier is indirectly transferred from one component to another via one or more intermediate structures, such as circuit elements, separating the components.

“Dielectric” refers to a non-conducting or insulating material. In an embodiment, an inorganic dielectric comprises a dielectric material substantially free of carbon. Specific examples of inorganic dielectric materials include, but are not limited to, silicon nitride and silicon dioxide.

“Dopant” refers to ions, atoms, compounds, or any aggregates or combinations of these that are introduced into a material, usually in small quantities, to affect the material's chemical, electrical or physical properties. As used herein dopants include, atoms, compounds, or any aggregates or combinations of these that are introduced in a semiconductor to affect the semiconductor's electrical characteristics, such as the semiconductor's electrical conductivity and resistance. Dopants useful herein include p-type dopants such as boron, n-type dopants such as phosphorous, antimony and arsenic, and combinations of n-type dopants and p-type dopants.

“Polymer” refers to a macromolecule composed of repeating structural units connected by covalent chemical bonds or the polymerization product of one or more monomers, often characterized by a high molecular weight. The term polymer includes homopolymers, or polymers consisting essentially of a single repeating monomer subunit. The term polymer also includes copolymers, or polymers consisting essentially of two or more monomer subunits, such as random, block, alternating, segmented, graft, tapered and other copolymers. Useful polymers include organic polymers or inorganic polymers and may be in amorphous, semi-amorphous, crystalline or partially crystalline states. Cross linked polymers having linked monomer chains are particularly useful for some applications. Polymers useable in the methods, devices and device components include, but are not limited to, plastics, elastomers, thermoplastic elastomers, elastoplastics, thermostats, thermoplastics and acrylates. Exemplary polymers include, but are not limited to, acetal polymers, biodegradable polymers, cellulosic polymers, fluoropolymers, nylons, polyacrylonitrile polymers, polyamide-imide polymers, polyimides, polyarylates, polybenzimidazole, polybutylene, polycarbonate, polyesters, polyetherimide, polyethylene, polyethylene copolymers and modified polyethylenes, polyketones, poly(methyl methacrylate, polymethylpentene, polyphenylene oxides and polyphenylene sulfides, polyphthalamide, polypropylene, polyurethanes, styrenic resins, sulfone based resins, vinyl-based resins, rubber (including natural rubber, styrene-butadiene, polybutadiene, neoprene, ethylene-propylene, butyl, nitrile, silicones), acrylic, nylon, polycarbonate, polyester, polyethylene, polypropylene, polystyrene, polyvinyl chloride, polyolefin or any combinations of these.

“Elastomer” refers to a polymeric material which can be stretched or deformed and return to its original shape without substantial permanent deformation. Elastomers commonly undergo substantially elastic deformations. Useful elastomers include those comprising polymers, copolymers, composite materials or mixtures of polymers and copolymers. Elastomeric layer refers to a layer comprising at least one elastomer. Elastomeric layers may also include dopants and other non-elastomeric materials. Useful elastomers useful include, but are not limited to, thermoplastic elastomers, styrenic materials, olefenic materials, polyolefin, polyurethane thermoplastic elastomers, polyamides, synthetic rubbers, PDMS, polybutadiene, polyisobutylene, poly(styrene-butadiene-styrene), polyurethanes, polychloroprene and silicones. In some embodiments, an elastomeric stamp comprises an elastomer. Exemplary elastomers include, but are not limited to silicon containing polymers such as polysiloxanes including poly(dimethyl siloxane) (i.e. PDMS and h-PDMS), poly(methyl siloxane), partially alkylated poly(methyl siloxane), poly(alkyl methyl siloxane) and poly(phenyl methyl siloxane), silicon modified elastomers, thermoplastic elastomers, styrenic materials, olefenic materials, polyolefin, polyurethane thermoplastic elastomers, polyamides, synthetic rubbers, polyisobutylene, poly(styrene-butadiene-styrene), polyurethanes, polychloroprene and silicones. In an embodiment, a flexible polymer is a flexible elastomer.

“Conformable” refers to a device, material or substrate which has a bending stiffness sufficiently low to allow the device, material or substrate to adopt a desired contour profile, for example a contour profile allowing for conformal contact with a surface having a pattern of relief or recessed features. In certain embodiments, a desired contour profile is that of a tissue in a biological environment, for example heart tissue.

“Low modulus” refers to materials having a Young's modulus less than or equal to 10 MPa, less than or equal to 5 MPa, or optionally less than or equal to 1 MPa and optionally for some applications less than or equal to 0.1 MPa.

“Young's modulus” and “modulus” are used interchangeably and refer to a mechanical property of a material, device or layer which refers to the ratio of stress to strain for a given substance. Young's modulus may be provided by the expression;

$\begin{matrix} {{E = {\frac{({stress})}{({strain})} = {\left( \frac{L_{0}}{\Delta\; L} \right)\left( \frac{F}{A} \right)}}},} & (I) \end{matrix}$ where E is Young's modulus, L₀ is the equilibrium length, ΔL is the length change under the applied stress, F is the force applied and A is the area over which the force is applied. Young's modulus may also be expressed in terms of Lame constants via the equation:

$\begin{matrix} {{E = \frac{\mu\left( {{3\;\lambda} + {2\;\mu}} \right)}{\lambda + \mu}},} & ({II}) \end{matrix}$ where λ and μ are Lame constants. High Young's modulus (or “high modulus”) and low Young's modulus (or “low modulus”) are relative descriptors of the magnitude of Young's modulus in a given material, layer or device. In some embodiments, a high Young's modulus is larger than a low Young's modulus, preferably 10 times larger for some applications, more preferably 100 times larger for other applications and even more preferably 1000 times larger for yet other applications. “Inhomogeneous Young's modulus” refers to a material having a Young's modulus that spatially varies (e.g., changes with surface location). A material having an inhomogeneous Young's modulus may optionally be described in terms of a “bulk” or “average” Young's modulus for the entire layer of material.

“Biocompatible” refers to a material that does not elicit an immunological rejection or detrimental effect when it is disposed within an in-vivo biological environment. For example, a biological marker indicative of an immune response changes less than 10%, or less than 20%, or less than 25%, or less than 40%, or less than 50% from a baseline value when a biocompatible material is implanted into a human or animal. Similarly, “bioresorbable” refers to a biocompatible material that is configured for transient function, and after a certain time period, to be removed from the implant site by natural chemical processes, including breakdown with exposure to the biological environment and biofluid.

“Bioinert” refers to a material that does not elicit an immune response from a human or animal when it is disposed within an in-vivo biological environment. For example, a biological marker indicative of an immune response remains substantially constant (plus or minus 5% of a baseline value) when a bioinert material is implanted into a human or animal.

Described herein are conformable electrophysiology interface data acquisition and/or stimulating devices and related methods for acquiring electrophysiology data at high-speed and high-resolution. The devices disclosed herein include devices useful for diagnosing and treating medical conditions in real time and with high spatial precision. The disclosed devices and methods also include those suited for monitoring electrical, of tissues in-vivo as they undergo motion, for example the tissue of a beating heart or brain swelling or deformation associated with intra-cranial pressure changes. The disclosed devices and methods further include those especially suited for monitoring electrical characteristics of tissues having nonplanar surfaces.

FIG. 1 illustrates an implantable and bioresorbable medical device comprising a bioresorbable substrate 10 (resorbable substrate of PLGA) and an electronic circuit 20 supported thereon. At least a portion of the electronic circuit corresponds to a membrane of silicon 30 (e.g., highly doped Si NMs) including a patterned membrane (see, e.g., FIG. 7A). A portion of the silicon membrane corresponds to dissolvable electrodes 40. An insulation layer 190 may electrically insulate interconnects 200 that electrically connect electrodes to external connections. The inset is a close-up view of the distal end of the device illustrating the electrodes as terminal pads 210 that are Si membrane portion not covered with the insulator layer 190.

Various other components of the device are further illustrated in FIG. 5A. Bioresorbable substrate 10 formed from resorbable PLGA supports a silicon membrane 30, including a doped silicon membrane, and related electronic circuit components. Illustrated are layers of SiO₂ (gate oxide) as a gate dielectric 80, with passages to correspond to exposed silicon 150. Metal (Mo) in a thin film 70 and an interlayer dielectric (ILD) 90 formed of SiO₂/Si₃N4/SiO₂ with the gate dielectric can form a MOSFET. A second thin layer of metal 120 can be used to define, for example, column select lines 125 (see, e.g., FIG. 24). An encapsulation layer 130, may cover the system, with passages 140 in alignment with underlying silicon to define active regions that correspond to an array of dissolvable electrodes. Additional geometry is illustrated in FIG. 5B, with active regions 160 at a distal end and separated from external electrical connectors 165 by a longitudinal distance 170. Vertical interconnects 180, including vias, may connect electrodes to backplane transistors.

A single unit cell of the multiplexed array 50 of dissolvable electrodes 40 is illustrated in FIG. 22. To facilitate multiplexing, buffer transistor 100 and multiplexing transistor 110 are electrically connected to an electrode.

Bioresorbable silicon electronics: The devices provided herein offer unprecedented opportunities to deploy advanced implantable monitoring systems that eliminate risks, cost and discomfort associated with surgical extraction. Applications include post-operative monitoring and transient physiologic recording after percutaneous or minimally invasive placement of vascular, cardiac, orthopedic, neural or other devices. Present herein are examples of these materials in both passive and actively addressed arrays of bioresorbable silicon electrodes with multiplexing capabilities, that record in vivo electrophysiological signals from the cortical surface and the subgaleal space. The devices detect normal physiologic and epileptiform activity, both in acute and chronic recordings. Comparative studies show sensor performance comparable to standard clinical systems and reduced tissue reactivity relative to conventional clinical electrocorticography (ECoG) electrodes. This technology offers general applicability in neural interfaces, with additional potential utility in treatment of disorders where transient monitoring and modulation of physiologic function, implant integrity and tissue recovery or regeneration are required.

Neurophysiologic monitoring is commonly used for diagnosing and treating neurological disorders such as epilepsy, Parkinson's disease, depression, chronic pain and disorders of the peripheral nervous system^(1,2). Such capabilities are critically important for mapping and monitoring brain function during and in preparation for resective neurosurgery³, such as for epilepsy and tumors, for assisting in neurodevice placement, such as for Parkinson's disease⁴, epilepsy⁵, and depression, and for guiding surgical procedures on complex, interconnected peripheral nerve structures such as the brachial, lumbar and sacral plexi². Related functionality is also increasingly leveraged during intravascular procedures, such as aneurysm coiling⁶, stent placement⁷, AVM embolization⁸, and endoscopic operations. Post-procedure monitoring typically occurs in an intensive care unit (ICU), where a variety of devices record physiologic activity, typically with limited temporal and spatial sampling, directly at the regions of interest, simply because these are exposed and accessible during surgery⁹. Intracranial monitors for postoperative seizures and recovery of brain function after surgery would also be useful, and potentially more sensitive than scalp monitoring¹⁰. These clinical needs motivate efforts to develop technologies for neurophysiologic monitoring that incorporate inorganic and organic nanomaterials in flexible formats¹¹⁻²⁰. Although it would be desirable for neuromonitoring in the ICU to offer the same high fidelity, high resolution performance as is available in the operating room, the morbidity and cost of associated with additional surgeries to remove implanted recording devices preclude this possibility in general practice. In certain cases, such as in invasive intracranial electrocorticographic monitoring for epilepsy surgery, recording electrodes remain in place for one to three weeks to localize epileptic networks²¹. Here, removal occurs in a second procedure, often with resection of brain involved in generating seizures. In other cases, electrodes are placed in staging procedures that do not end in resection, but rather are done for broad lateralization in preparation for more extensive implants or placement of implantable devices. Here, a second procedure to remove implants adds cost and risk. Recent evidence suggests that 1-3 months of ambulatory intracranial recording may be required to adequately localize seizures for epilepsy surgery or device placement, a period prohibitively long for current in-hospital approaches²². Using bioresorbable electrodes for such studies would eliminate the danger and cost of removing standard electrodes at the end of this period, during which standard devices may become fibrosed or adherent to underlying tissues. An ideal scenario would involve placement of temporary, bioresorbable monitoring devices capable of providing continuous streams of data for guiding medical care over predetermined periods of time before dissolving. Below we present a new class of technology that offers this mode of operation, with spatio-temporal resolution that matches or exceeds any existing alternative.

Recently reported bioresorbable sensors of pressure and temperature in the intracranial space provide distinct, complementary capabilities in single-point measurements of non-electrical characteristics of the cerebrospinal fluid in the intracranial space²³. The results presented here introduce materials and device designs for direct electrical interfaces to the brain itself, including bioresorbable electrodes and multiplexing electronics for high speed spatio-temporal mapping of biological processes. The platform builds on recently described technologies that exploit nanomembranes of device-grade, monocrystalline silicon (Si NMs) as the semiconductor foundation of a high performance class of electronic systems. The key enabling chemistry involves hydrolysis of Si NMs upon immersion in biofluids, to yield end products that are biocompatible. The results presented here indicate that Si NMs, at high levels of doping²⁴, can additionally serve as the neural recording electrodes themselves, as a stable, yet ultimately transient, measurement interface. In addition to their established bioresorbability, the nanoscale thicknesses of Si NMs, when deployed with thin substrates, interconnect metals and dielectrics, yield devices with levels of mechanical flexibility necessary for conformal contact and chronically stable interfaces with neural tissues. The following describes means to exploit these concepts in materials, devices and system-level examples of bioresorbable Si electronic interfaces to the brain, with examples in passive and active matrix addressed recording in vivo. Evaluations include capture of ECoG and subdermal encephalograms (EEG) in live, awake animal models, where Si NMs serve as active materials both for the recording interface and for the backplane transistors that allow high speed multiplexed addressing across arrays of channels. Comprehensive in vitro and in vivo studies establish that these systems provide accurate and reproducible measurements of neural signals and physiological activity for acute (˜hours) and chronic (up to 33 days) use. Biocompatibility studies reveal no overt tissue reactions compared to clinically approved commercial ECoG electrodes.

FIG. 1A provides an exploded schematic diagram (left) of a magnified optical microscope image of the active sensing and the passivation regions (right) of a simplest embodiment of these concepts: a thin, flexible electrode array based on phosphorus doped (impurity concentrations: ˜10²⁰/cm³) collection of Si NM (thickness ˜300 nm) structures. Here, a layer of SiO₂ (thickness ˜100 nm) insulates the connection traces to isolate them from bio-fluids and adjacent tissue. The terminal pads comprise exposed Si, as the direct neural interface. A flexible sheet of the bioresorbable polymer poly(lactic-co-glycolic acid, PLGA, thickness ˜30 μm) serves as the substrate. This array (3×4 mm²) allows chronic recordings from rat cortex at four measurement sites, each with dimensions of 250×250 μm². Such small arrays serve effectively in demonstrator experiments and studies of the fundamental issues in the materials science. The materials and fabrication schemes do, however, align with those used in the semiconductor industry and are, as a result, immediately scalable to much larger areas, higher channel counts and smaller/larger electrode sizes. As an illustration, FIG. 1B (bottom frames) presents a passive array that includes 256 independent channels, in a 16×16 configuration, with an overall area of 3 cm×3.5 cm. Multiplexing architectures, described subsequently, provide routes to scaling to even higher numbers of channels. The fabrication steps appear in the methods section and in FIG. 7A-7B. The lot and functional electrode yields are ˜100% and >90%, respectively. FIG. 1B and FIG. 8 show micrographs of completed arrays. FIG. 1B (bottom) shows a scaled version of this same basic device architecture that includes 256 independent channels.

Placing an array onto a hydrogel substrate (FIG. 1C) and immersing the system in phosphate-buffered saline (PBS) at physiological pH (7.4) and at room temperature enables characterization of each of the electrodes by electrochemical impedance spectroscopy (EIS), across a range of frequencies most relevant to the studies described subsequently. In the recording of brain signals, the electrodes transduce ionic currents in the electrolyte to an electric current in the measurement system. The contact between an electrode and tissue has associated electrical impedance, where reductions in the impedance decrease the noise level, thereby increasing the signal to noise ratio (SNR) of the recordings^(19,25). The data in FIG. 1D correspond to the impedance (IZI) of each channel in the array, along with the response of a gold (Au) electrode with the same dimensions. The EIS data for Si can be fit to an equivalent Randles circuit model (FIG. 9A) that includes a double layer capacitance (C_(PE)) in parallel with a charge transfer resistance (R_(CT)), all of which is in series with a resistance (R_(S)) that corresponds to the surrounding electrolyte solution. This model quantitatively captures the EIS data for both Au (without the space charge layer) and Si electrodes, as shown in FIG. 9B. The fitted values of C_(PE) are ˜2.5 μF/cm² and ˜10 μF/cm² for Si and Au, respectively; both values are in a range consistent with the literature^(26,27.) The space charge layer lowers the capacitance of the Si electrode²⁸, causing the difference in capacitances for Au and Si electrodes (FIG. 1D). More details of in vitro experiments of the Si electrodes are described below and FIGS. 10-13.

In Vitro Experiments of Phosphorus Doped Si NM Electrodes.

Results of impedance measured on devices constructed using Si NMs with different dopant species and concentrations (phosphorus, between ˜10¹⁷ and ˜10²⁰/cm³; and boron, at ˜10²⁰/cm³) are comparable at all frequencies, up to ˜1 kHz. (FIGS. 10 and 11). The impedances measured from Si NMs with different thicknesses across a relevant range also show similar values (FIG. 12), thereby suggesting an ability for continuous, reliable neural recording even as the electrodes dissolve over time. The doping level and the thickness do, however, strongly affect the time for complete dissolution, where increasing the level and thickness increases the lifetime. The impedance decreases, as expected, inversely with the areas of the electrodes (phosphorous, ˜10²⁰/cm³), as illustrated in the data of FIG. 13 for dimensions of 200×200 μm² (A1), 300×300 μm² (A2), 400×400 μm² (A3), 500×500 μm² (A4).

The slow, controlled dissolution of Si NMs is an important aspect in their use as bioresorbable neural interfaces. Bioresorbable metals are less attractive options due to their comparatively fast dissolution kinetics, and tendency to crack, fragment and flake during the process. Si dissolves under physiological conditions by hydrolysis to yield silicic acid, at rates that depend strongly on ionic content of the surrounding solution, pH, temperature and other factors, including the doping level. Specifically, Si forms neutral ortho-silicic acid Si(OH)₄ through an initial oxidation step to SiO₂ or through a direct equilibrium Si+4H₂O

Si(OH)₄+2H₂ ^(29,30). FIG. 1E illustrates the dissolution kinetics for highly boron and phosphorus doped (concentration of ˜10²⁰/cm³) Si NMs (˜300 nm thick) in artificial cerebrospinal fluid (aCSF, pH 7.4) at physiological temperature (37° C.), evaluated by measuring the thicknesses at different time points by profilometry (Dektak, USA). Observations indicate that dissolution occurs in an exceptionally controlled, predictable process, without cracks, flakes, particulates or reduction in surface smoothness that often occurs in dissolution of metals. The dissolution rate exhibits a constant, thickness independent value of ˜11 nm/day for these conditions. The dissolution characteristics of the other materials in the system, which for the case of the simple device in FIG. 1A-1G are SiO₂ and PLGA, are also important, although less critical than the Si NMs due to their passive role in the device operation. Measurements indicate that SiO₂ and PLGA (75:25)³¹ dissolve in biofluids at 37° C. at rates of ˜8.2 nm/day (FIG. 14), and complete dissolution time scales of ˜4-5 weeks, respectively. Results of accelerated dissolution tests appear in FIG. 1G as a series of images of a complete device collected at various times after immersion in PBS pH 10 at 37° C. We estimate that the current device designs and material choices allow complete dissolution of the device in 2 months. Si and SiO₂ will dissolve within a month and 2 weeks, respectively, followed by PLGA. PLGA will dissolve in ˜4-5 weeks. The materials parameters (i.e., thicknesses, doping levels for the Si, and ratio of lactide to glycolide for the PLGA) can be adjusted to achieve desired dissolution times.

For conformal contact against the curved surface of the brain, thin geometries and optimized mechanical layouts are important. Three dimensional finite element modeling (FEM) reveals distributions of principle strain for bending perpendicular to the interconnect direction, as in FIG. 1F (left). Based on the layouts and the mechanical moduli, the maximum strains in the SiO₂, Si and PLGA are less than 0.03% for a bending radius of 1 mm, corresponding to the linear elastic regime for each of these materials. An optical image of a device wrapped around a glass rod with a radius of curvature of ˜2 mm appears in FIG. 1F (right). Measurements before and after bending show negligible differences in impedance, consistent with expectation based both on FEM and analytical modeling results (FIG. 15).

In vivo neural recording experiments involved the bioresorbable devices of FIG. 1A-1G in adult rat animal models anesthetized and placed in a stereotaxic apparatus. A craniotomy exposed a 4×8 mm² region of cortex in left hemisphere (FIG. 2A), to allow positioning of a device on an area of the cortical surface next to a standard stainless steel microelectrode (7,850 μm²) as a control for recording physiological oscillations under isofluorene anesthesia. FIG. 2B shows representative sleep spindle activity captured by one of the channels in the bioresorbable array and the control electrode. FIG. 16A-16B show similar data for brain waves recorded during transition to deep anesthesia (FIG. 16A) and K-complexes (FIG. 16B) measured under anesthesia. Representative examples of pre-ictal and ictal-like spiking epileptiform activity induced by application of crystals of bicuculline methoxide recorded by the bioresorbable electrode and the control electrode appear in FIG. 2C and FIG. 2D, respectively. The frequency of the pre-ictal spikes (FIG. 2C) increases and the inter-spike duration decreases as the time progresses, terminating into after discharges and ictal-like early epileptic discharges (FIG. 2D). The bioresorbable arrays can also be utilized as subdermal implants for high fidelity, recording of EEG and evoked potentials. Devices implanted on periosteum as described in FIG. 2E and FIG. 17 yielded reliable recordings of theta waves (highlighted in power spectral analysis) and sleep spindles (FIG. 2F). Collectively, the results demonstrate that bioresorbable recording platforms can capture reliable physiological or pathological activity both intracortically and subdermally.

Chronic tests of ECoG recording indicate long-term stability in operation, where devices with increased thicknesses of SiO₂ (˜300 nm) and Si NMs (˜1000 nm) survive for more than one month. Such studies used a miniature interface board connected to the device via a flexible interconnect cable to a headstage (FIG. 18) designed for use with rats. Details are explained in the Methods section. FIG. 3A-3G summarizes representative cortical potentials recorded by three electrodes in the bioresorbable array and by a nearby screw electrode as a control, captured on Days 1, 8, 15, 30, 32 (FIG. 19), and 33 measured from the time of the surgical implantation. FIGS. 3A, 18 and 20 describe the surgical procedures and the post-surgical setups used in freely moving rats, respectively. ECoG potentials show physiological signals and brain oscillations with various temporal and spatial differences. High-amplitude seizure-like rhythmic spike discharges (FIG. 3G) appear occasionally, consistent with absence-like seizure activity observed in Long Evans Rats³²⁻³⁴. By all functional metrics (e.g. signal to noise ratio, ability to measure delta, theta, alpha, gamma, spindles and sometimes epileptic spikes), the devices operate in a stable fashion, largely without change in performance throughout the month of the study, until sudden failure, likely due to the development of an open circuit state in the vicinity of the interconnects. After day 33, signals from the bioresorbable device disappear; while those form the control persist, consistent with dissolution of at least some critical component of the device. For epilepsy patients the clinically relevant operational lifetime is several weeks. Here, bioresorbable devices could be embedded into particular clinical devices to monitor for early signs of failure during critical post-operative periods, such as measuring pressure and flow after intravascular aneurysm occlusion (coiling), placement of aortic or other vascular grafts, or procedures to seal cerebrospinal fluid (CSF) leaks. Currently monitoring is based upon clinical examination, or requires interventional radiology that is invasive, expensive and impractical for continuous monitoring over days to months.

Understanding the reactive tissue response is important in assessing the potential for use in such clinical applications³⁵. Tissue inflammation, encapsulation of the electrodes in fibrous tissue (glial scar) and neuronal death in the vicinity of the electrode are the most important issues related to clinical translation³⁶⁻³⁸. Studies of tissue reactions of bioresorbable electrode arrays involved chronic implants in 14 animals, with Pt electrodes cut into similar geometries from clinical subdural grids (Ad-Tech Medical Inc) as controls, as shown in FIG. 21. FIG. 4A-4B summarizes the results obtained according to procedures outlined in the methods section. Double label immunohistochemistry for GFAP and Iba-1 reveal glial cell activation at 4 weeks post-implant (FIG. 4A-4B). In both control and bioresorbable devices, moderate subpial gliosis occurs at the implantation site, when compared to the control contralateral hemisphere. No significant astrogliosis is noted at distant sites within the ipsilateral hemisphere. Iba-1 immunohistochemistry demonstrates the presence of both resting ramified, as well as round activated microglia underneath the control electrode, which extends to the superficial layers I-III. In contrast, at the implantation site of the bioresorbable electrode, microglial cells show an almost exclusively ramified morphology. The contralateral side in both groups exhibits no microglial reaction. The sham-operated control demonstrates a similar moderate subpial gliosis, but with no change in microglial densities or morphology.

Actively multiplexed device designs enable high-resolution, high channel count neural interfaces by minimizing the number of wires needed for external data acquisition. In this context, Si NMs provide not only an excellent choice for the electrodes but also for the backplane electronics, including the necessary switching and buffer transistors as a scalable pathway toward systems with increased numbers of channels and area coverage. A fully bioresorbable design appears in FIG. 5A; a sequence of images at various stages of the fabrication appear on the right. This embodiment uses 128 n-channel metal-oxide-semiconductor field-effect transistors (MOSFETs), with Molybdenum (Mo) for the source, drain and gate electrodes, and SiO₂ (˜100 nm) for the gate dielectrics. Additional layers of Mo and a trilayer of SiO₂ (˜300 nm)/Si₃N₄ (˜400 nm)/SiO₂ (˜300 nm) form interconnects and interlayer dielectrics (ILD), respectively. A second layer of Mo (˜300 nm) serves as column selects and additional sensing electrode pads. Another trilayer provides a blanket encapsulating layer that has openings only at the locations of the Mo interface electrodes. The amount of materials in a single device with active multiplexed addressing are 100 mcg of Mo, 1.43 mcg of Si, 306 mcg of SiO₂, 264 mcg of S₃iN₄, and 27 pg of P. For comparison, the daily intake limits, average daily intake values, and daily production of such materials appear in TABLE 1. The chemistry, dissolution kinetics and biocompatibility of each of the constituent materials can be found elsewhere³⁹⁻⁴⁶. The lot and functional electrode yields are ˜10-20% and ˜80%, respectively. Failures arise from leakage currents associated with pinholes in the encapsulating layer, introduced by particulate contamination in our academic cleanroom facilities. FIG. 5B presents photographs of a device, wrapped around a cylindrical tube, with an inset that shows arrays of active electrodes. FIG. 5C summarizes the electrical properties of a representative n-type MOSFET, where the mobility and on/off ratio are ˜400 cm² V⁻¹ and ˜10⁸, respectively, as calculated using standard field-effect transistor models. FIG. 5D shows in vitro measurements on a representative unit cell. The output response was consistent with the input signal, thereby indicating proper operation. Details of in vitro experiments are provided below and in FIGS. 21-26.

Operation of the Multiplexing on a Representative Unit Cell.

FIGS. 22-24 summarize the key aspects of the designs of circuits that incorporate these transistors for multiplexed addressing. The approach involves two transistors per unit cell^(12,14), in which a buffer transistor connects to the interface electrode to provide buffering of measured biopotentials, and a multiplexing transistor allows electrodes in a given column to share a single output wire. The surface electrodes appear in the top layer, where they come into physical contact with the brain; they connect to the underlying backplane circuit through vertical interconnect access holes (vias). An active shielding scheme described in FIG. 24 improves the signal to noise ratio of the system by reducing the parasitic capacitance and increases the gain of each site of the electrodes. The operation involved successive application of 3V (V_(r)) to the gate of the multiplexing transistor when a particular row was activated and −3V (V_(r)) when the row was not selected (FIGS. 22 and 23). A constant current of 4 μA was used to bias the column output and complete the source follower amplifier. The output voltage (V_(c)) was high-pass filtered to have an average DC bias of 2V and connected to the column power source line (V_(as)). By using analog feedback, the negative effects of parasitic capacitance in the drain of the buffer transistor are reduced and the AC signal gain of the electrode array is improved. A 50 Hz, 200 mV (peak to peak) sinusoidal waveform was applied to a metal reference electrode immersed in PBS at pH 7.4 and recorded from the active electrode array (FIG. 25). During multiplexed sampling, driving the row select signal selects a single row of electrodes at a time. This scheme allows the unit cells in the corresponding row to drive the column output lines which connect to a high-speed analog to digital converter. Row select signals are rapidly cycled to sample all electrodes on the array. The entire device connects to an external data acquisition (DAQ) system through a zero insertion force (ZIF) connector with 26 contact.

FIG. 5E shows a sequence of images during accelerated dissolution in PBS pH 12 at 37° C. PECVD Si₃N₄ and Mo^(40,41) dissolves in biofluids at pH 7.4 at 37° C. at a rate of ˜5.1 nm/day (FIG. 14) and ˜16-25 nm/day, respectively. This system involves ˜1.3 μm, ˜800 nm, ˜300 nm, ˜600 nm and ˜30 μm thick layers of PECVD SiO₂, Si₃N₄, Si, Mo and PLGA, respectively. PLGA, Si, and Mo in biofluids at 37° C. dissolve completely within in ˜4-6 weeks. Both SiO₂ and Si₃N₄, dissolve in 6 months under the same conditions. FIG. 26 shows results of measurements of gain across the array and cumulative leakage current for a representative device immersed in PBS at pH 7.4. The average gain and yield were 94% and 100%, respectively.

FIG. 6A-6G provides details on in vivo recordings with a bioresorbable, multiplexed recording array. The leakage current is ˜10 nA. The 64-electrode array was placed on the cortical surface of the left hemisphere of an anesthetized rat in a stereotaxic apparatus (FIG. 27). Picrotoxin was applied topically to induce epileptiform activity, just prior to the placement of the array. The data reveal epileptic spikes and discharges that last ˜1-3 s and repeat every ˜10-15 s. A set of different epileptic spikes (clockwise spiral, lower right to upper left diagonal, upper left to lower right diagonal, and right to left sweep) is shown in FIG. 6A as representative recordings. The sequence of eight movie frames corresponding to each spike (FIG. 6B) clearly reveals the propagation of neural waves and associated spatial-temporally resolved patterns. The delay maps represent the latency of the spike's peak at each site (FIG. 6C). Each spiking activity shows a distinctive spatial flow indicated by the yellow arrow in each delay map. RMS power maps, corresponding to each representative spike (FIGS. 6c and 28) show the spatially resolved patterns.

In addition to epileptiform activity, spatial distributions of low amplitude evoked cortical activity can be captured using the same device. Somatosensory evoked potential (SSEP) experiments were conducted in anesthetized rats using the bioresorbable multiplexed array on the surface of the exposed barrel cortex. Evoked potentials were produced by stimulating two different whiskers (B1 and E3, FIG. 6D), corresponding to the barrel cortex and estimated relative location (FIG. 6E). The temporally resolved patterns of the evoked potentials are shown in FIG. 6F. The spatial distribution of the amplitude of the evoked potentials measured at the cortical surface by the array is consistent with the relative location of the activated whiskers on the barrel cortex as described with the color map (FIG. 6G). These results collectively demonstrate an ability to record stimulus evoked and drug-induced neural activity with high SNR. The same materials and device architectures can be easily adapted to larger areas and increased channel counts with potential for use in large animal models and, in the future, for clinical monitoring applications.

The concepts introduced here form a robust foundation of capabilities in bioresorbable implantable electrode technology for various clinical problems, ranging from post-operation monitoring of brain activity to electrical monitoring of skeletal muscles or organ function. In all cases, the thin, flexible form factors minimize mechanical injury associated with implantation and chronic use. The use of Si as the active semiconductor material aligns the technology consumer electronics industry with the natural capacity to scale to higher densities of electrodes and larger areas.

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Fabrication of Passive Electrode Arrays.

Fabrication of the passive electrode arrays began with solid state phosphorus doping (PH-1000N Source, Saint Gobain, USA, 1000° C. for 10 minutes) of p-type device Si on a Si on insulator (SOI, top Si ˜300 nm, SOITEC, France) wafer. Removing the buried oxide layer of the SOI by wet etching with concentrated HF released the device Si as a Si NM, retrieved with a slab of the elastomer poly(dimethylsiloxane) (PDMS) and transfer-printed to a spin-cast bilayer of poly(methylmethacrylate) (PMMA, ˜800 nm thick) and polyimide (PI, ˜300 nm thick) on a Si wafer. Photolithography and reactive ion etching (RIE) defined a pattern of electrodes and interconnects in the Si NMs. Plasma enhanced chemical vapor deposition (PECVD) formed a layer of SiO₂ (thickness 100 nm) as encapsulation. Patterned etching with buffered oxide etchant removed the SiO₂ from the electrode regions. Spin casting and patterning a top coating of PI (˜300 nm thick) placed the Si NM electrodes and interconnects near the neutral mechanical plane. Patterning a mesh structure across the multilayer (i.e. PI, SIO₂, PI and PMMA) by RIE followed by immersion in buffered oxide etchant exposed the base layer of PMMA to allow its dissolution in acetone. Retrieval onto a slab of PDMS enabled removal of the bottom exposed layer of PI by RIE. Transfer onto a film of PLGA (˜30 μm thick), facilitated by heating to temperatures close to the glass transition of the PLGA (55˜60° C., lactide/glycolide ratio of 75:25 composition), followed by elimination of the top layer of PI by RIE completed the fabrication. Bonding an ACF cable to the terminal regions of the Si NM interconnects yielded connection points for interfaces to external data acquisition (DAQ) systems.

Fabrication of Actively Multiplexed Electrode Arrays.

The fabrication began with growth of 200 nm of thermal oxide on a p-type SOI wafer (top Si ˜320 nm, SOITEC), photolithography and immersion in buffered oxide etchant to create a mask for solid state phosphorus diffusion (1000° C. for 6 minutes) to define the source and drain contacts. Releasing, retrieving and transferring the doped Si NMs onto a temporary substrate, consisting of Si wafer with a bilayer coating of PI/PMMA, followed procedures similar to those described for passive electrode arrays. Photolithography and RIE etching patterned the Si NMs into geometries for an 8×8 array of unit cells, each consisting of two transistors connected in series for purpose of actively multiplexed readout. A thin layer of SiO₂ (PECVD at 220° C., thickness ˜100 nm) served as the gate dielectric. Buffered oxide etching through a photolithographically patterned mask formed openings through the SiO₂ to expose the source and drain contact regions. Photolithography and lift off in acetone defined a patterned layer of Mo (sputter deposited, thickness ˜300 nm) for the gate electrodes and metal interconnects. Deposition of a trilayer of SiO₂ (˜300 nm)/Si₃N₄ (˜400 nm)/SiO₂ (˜300 nm) by PECVD formed the interlayer dielectric. Photolithography and buffered oxide etching created vertical interconnect access (via) holes for electrical connections between layers. An additional layer of Mo (thickness ˜300 nm) patterned by photolithography and liftoff defined column select lines. Another trilayer of SiO₂ (˜300 nm)/Si₃N₄ (˜400 nm)/SiO₂ (˜300 nm) served as encapsulation, with openings at the locations of the sensing electrodes and peripheral contact pads for interfacing to an external DAQ system. A spin-cast layer of PI served as device passivation. Selective RIE and buffered oxide etching through these multilayer stacks (diluted PI/trilayers of inorganic materials/trilayers of inorganic materials/Diluted PI) formed mesh structures that enabled release of active layers from the temporary substrate by dissolving the PMMA layer in acetone. Transfer printing steps followed, according to procedures similar to those for the passive electrode fabrication.

In Vivo Acute Recordings of Epileptiform Activity.

The in vivo data FIG. 2A-2G is representative of four different acute experiments, each of which lasted 5-6 hours. The procedures, which were approved by the Institutional Care and Use Committee of the University of Pennsylvania, involved an anaesthetized rat with its head fixed in a stereotaxic apparatus. Wild-type, adult Long Evans male and female rats were used. The animal was anesthetized with initially ketamine/xylazine and then isoflurane throughout the craniotomy and neural recordings. A craniotomy exposed a 4×8 mm region of cortex in either left or tight or in both hemispheres. All recordings were taken in reference to a distant stainless steel bone screw inserted through the skull during the surgery. A commercial stainless steel microwire electrode (˜100 um stainless steel wire from California Fine Wire) placed at 0.5 mm depth from the cortical surface in close proximity to the bioresorbable electrodes served as a control during acute recordings. Neural data was acquired by a FHC multi-channel neural amplifier (FHC Inc, Bowdoin, Me., USA) and an acquisition system (16 bit Axon Instruments Digidata 1322A, Axon Instruments, Foster City, Calif.). Recordings were high pass filtered at 0.1 Hz. Neural recording data were analyzed offline using Clampfit software (Axon Instruments) and custom Matlab software for neural signal analysis.

In Vivo Acute Recordings of Evoked Responses by Whisker Stimulation.

The following procedures were approved by the Institutional Care and Use Committee of the University of Pennsylvania. One 150-g, Sprague-Dawley rat was anesthetized with a ketamine (60 mg/kg), dexdomitor (0.25 mg/kg) solution and placed in a stereotaxic frame. A craniotomy was performed to expose the right barrel cortex. A skull screw was placed in the left frontal bone to serve as the reference electrode for the recordings. The recording array was placed over the exposed cortical surface. A pair of needle stimulating electrode were inserted into the left mystacial pad at various locations. Brief electrical currents (˜250-600 μA, 1 ms/phase, biphasic pulse) were passed between the electrodes to activate the intrinsic muscles of the vibrissae, causing a visible protraction of the whiskers. Current amplitude and electrode spacing was adjusted for focal activation, usually 1-4 whiskers. Cortical potentials evoked by the whisker stimulation were recorded at 781.25 samples/s.

In Vivo Chronic Recordings.

An adult Long Evans rat was anesthetized with isoflurane and placed in a stereotactic frame (David Kopf Instruments Tujunga, Calif.). Body temperature was maintained with a heating blanket and the eyes were covered with ointment to prevent drying. The skull was exposed and a large craniotomy (4×8 mm²) was made between bregma and lambda and laterally to the midline. The electrode was placed on the exposed dura and a slurry of gel foam and saline was layered on top of the electrode. A screw electrode was placed contralaterally to the experimental array, with another such electrode placed posterior to lambda as a ground and reference. Additional screws were secured in the skull for anchoring. The skull and electrodes were then covered with dental cement and the connecting plug was secured on top. The rat was given meloxicam for postoperative pain and allowed to recover on a heating pad. The rat was given meloxicam daily for 3 days after surgery to minimize pain. After 1 week the animal was placed in a cage for video/EEG recording. EEG signals were collected continuously from 3 channels on the array and from the screw. The signals were amplified and low pass filtered at 600 Hz (Multichannel Systems, Reutlingen, Germany) and sampled at 2000 Hz with a 16 bit digitizer (National Instruments, Austin, Tex.). Data was acquired using a custom written MATLAB routine.

Chronic Evaluation of Immunohistochemistry.

Rats (n=14) were anesthetized and transcardiac perfusion was performed using phosphate buffered saline (PBS 10×, cat. #BM-220, Boston BioProducts, Ashland, Mass.), followed by 4% paraformaldehyde (PFA, cat. #BM-155, Boston BioProducts). Whole brains were then removed and post-fixed overnight at 4° C. in the same 4% PFA solution. Subsequently, fixed brains were cryoprotected in 30% sucrose (cat. #57-50-1, Sigma-Aldrich, Saint Louis, Mo.) at 4° C. and coronal sections were cut at 20 μm using a Leica CM3050 S cryostat (Leica Biosystems Inc.). Serial sections, spanning the entire craniotomy site, were mounted on charged slides and stored at −20° C. until use. For immunostaining, slides were first immersed in an antigen retrieval solution (0.1 M citrate buffer, pH 6.0, cat #ab64214, Abcam, Cambridge, Mass.) and placed in a water bath at 95° C. for 10 minute. After cooling, sections were rinsed in distilled water, incubated in a blocking solution containing 0.1% Triton X-100 (cat. #9002-93-1, Sigma-Aldrich) and 5% normal goat serum (cat. #GS-0500, Equitech-Bio Inc., Kerrville, Tex.) for one hour at room temperature (RT) and then incubated overnight at 4° C. with the following primary antibodies: anti-Glial Fibrillary Acidic Protein (GFAP, 1:1000, cat. #SMI-22R, Covance, Princeton, N.J.), and anti-ionized calcium binding adapter molecule 1 (Iba-1, 1:1000, cat. #019-19741, Wako Chemicals USA, Inc., Richmond, Va.). After 3×20-minute washes in PBS, sections were incubated with the corresponding fluorescent secondary antibodies (Alexa Fluor 488 goat anti-mouse IgG2b, 1:1000, cat. #A-21141, and Alexa Fluor 568 goat anti-rabbit IgG, 1:1000, cat. #A-11011, Invitrogen by Life Technologies, Grand Island, N.Y.). After the final washes (3×20 min in PBS), the slides were cover-slipped with an anti-fade medium containing the nuclear stain DAPI (Fluoromount-G+DAPI, cat. #0100-20, Southern Biotechnology, Birmingham, Ala.). Control sections were incubated with omission of one or both primary antibodies, adding only the secondary antibodies to exclude false-positive labeling. Slides were examined on an epifluorescence microscope (Zeiss Axioscope, Germany) and images were acquired with a 20× objective and a Spot RT3 digital camera, using the Spot Software 5.1 (Diagnostic Instruments, Sterling Heights, Mich.). Digital images were processed using Adobe Photoshop 12.0 (Adobe Systems, San Jose, Calif.).

SUPPLEMENTARY REFERENCES

-   1.     http://iom.nationalacademies.org/Activities/Nutrition/SummaryDRIs/DRI-Tables.aspx -   2. Pennington, J. A. T. Silicon in foods and diets Food. Addit.     Contam. 8, 97-118 (1991). -   3. Jugdaohsingh, R. et al. Dietary silicon intake and absorption.     Am. J. Clin. Nutr. 75, 887-893 (2002). -   4. Syracus research coporations. Toxicological profile for ammonia.     (2004). -   5. Kawahara, M, & Kato-Negishi, M. Link between aluminum and the     pathogenesis of Alzheimer's Disease: the integration of the aluminum     and amyloid cascade hypotheses. Int. J. Alzheimer's Dis. 2011,     276393 (2011). -   6. Jurkic, L. M., Cepanec, I., Pavelic, S. K., & Pavelic, K.     Biological and therapeutic effects of ortho-silicic acid and some     ortho-silicic acid-releasing compounds: new perspectives for     therapy. Nutr. Metab. 10, 2-12 (2013). -   7. Davenward, S. et al. Silicon-rich mineral water as a non-invasive     test of the ‘aluminum hypothesis’ in Alzheimer's disease. J     Alzheimers Dis. 33, 423-430 (2013).

STATEMENTS REGARDING INCORPORATION BY REFERENCE AND VARIATIONS

All references throughout this application, for example patent documents including issued or granted patents or equivalents; patent application publications; and non-patent literature documents or other source material; are hereby incorporated by reference herein in their entireties, as though individually incorporated by reference, to the extent each reference is at least partially not inconsistent with the disclosure in this application (for example, a reference that is partially inconsistent is incorporated by reference except for the partially inconsistent portion of the reference).

The terms and expressions which have been employed herein are used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments, exemplary embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims. The specific embodiments provided herein are examples of useful embodiments of the present invention and it will be apparent to one skilled in the art that the present invention may be carried out using a large number of variations of the devices, device components, methods steps set forth in the present description. As will be obvious to one of skill in the art, methods and devices useful for the present methods can include a large number of optional composition and processing elements and steps.

When a group of substituents is disclosed herein, it is understood that all individual members of that group and all subgroups are disclosed separately. When a Markush group or other grouping is used herein, all individual members of the group and all combinations and subcombinations possible of the group are intended to be individually included in the disclosure.

Every formulation or combination of components described or exemplified herein can be used to practice the invention, unless otherwise stated.

Whenever a range is given in the specification, for example, a size range, a temperature range, a time range, or a composition or concentration range, all intermediate ranges and subranges, as well as all individual values included in the ranges given are intended to be included in the disclosure. It will be understood that any subranges or individual values in a range or subrange that are included in the description herein can be excluded from the claims herein.

All patents and publications mentioned in the specification are indicative of the levels of skill of those skilled in the art to which the invention pertains. References cited herein are incorporated by reference herein in their entirety to indicate the state of the art as of their publication or filing date and it is intended that this information can be employed herein, if needed, to exclude specific embodiments that are in the prior art. For example, when composition of matter are claimed, it should be understood that compounds known and available in the art prior to Applicant's invention, including compounds for which an enabling disclosure is provided in the references cited herein, are not intended to be included in the composition of matter claims herein.

As used herein, “comprising” is synonymous with “including,” “containing,” or “characterized by,” and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps. As used herein, “consisting of” excludes any element, step, or ingredient not specified in the claim element. As used herein, “consisting essentially of” does not exclude materials or steps that do not materially affect the basic and novel characteristics of the claim. In each instance herein any of the terms “comprising”, “consisting essentially of” and “consisting of” may be replaced with either of the other two terms. The invention illustratively described herein suitably may be practiced in the absence of any element or elements, limitation or limitations which is not specifically disclosed herein.

One of ordinary skill in the art will appreciate that starting materials, biological materials, reagents, synthetic methods, purification methods, analytical methods, assay methods, and biological methods other than those specifically exemplified can be employed in the practice of the invention without resort to undue experimentation. All art-known functional equivalents, of any such materials and methods are intended to be included in this invention. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.

The following references relate generally to fabrication methods, structures and systems for making electronic devices, and are hereby incorporated by reference to the extent not inconsistent with the disclosure in this application.

Attorney Application Publication Publication Docket No. No. Filing Date No. Date Pat. No. Issue Date 145-03 US 11/001,689 Dec. 1, 2004 2006/0286488 Dec. 21, 2006 7,704,684 Apr. 27, 2010 18-04 US 11/115,954 Apr. 27, 2005 2005/0238967 Oct. 27, 2005 7,195,733 Mar. 27, 2007 38-04A US 11/145,574 Jun. 2, 2005 2009/0294803 Dec. 3, 2009 7,622,367 Nov. 24, 2009 38-04B US 11/145,542 Jun. 2, 2005 2006/0038182 Feb. 23, 2006 7,557,367 Jul. 7, 2009 43-06 US 11/421,654 Jun. 1, 2006 2007/0032089 Feb. 8, 2007 7,799,699 Sep. 21, 2010 38-04C US 11/423,287 Jun. 9, 2006 2006/0286785 Dec. 21, 2006 7,521,292 Apr. 21, 2009 41-06 US 11/423,192 Jun. 9, 2006 2009/0199960 Aug. 13, 2009 7,943,491 May 17, 2011 25-06 US 11/465,317 Aug. 17, 2006 — — — — 137-05 US 11/675,659 Feb. 16, 2007 2008/0055581 Mar. 6, 2008 — — 90-06 US 11/782,799 Jul. 25, 2007 2008/0212102 Sep. 4, 2008 7,705,280 Apr. 27, 2010 134-06 US 11/851,182 Sep. 6, 2007 2008/0157235 Jul. 3, 2008 8,217,381 Jul. 10, 2012 151-06 US 11/585,788 Sep. 20, 2007 2008/0108171 May 8, 2008 7,932,123 Apr. 26, 2011 216-06 US 11/981,380 Oct. 31, 2007 2010/0283069 Nov. 11, 2010 7,972,875 Jul. 5, 2011 116-07 US 12/372,605 Feb. 17, 2009 — — — — 213-07 US 12/398,811 Mar. 5, 2009 2010/0002402 Jan. 7, 2010 8,552,299 Oct. 8, 2013 38-04D US 12/405,475 Mar. 17, 2009 2010/0059863 Mar. 11, 2010 8,198,621 Jun. 12, 2012 170-07 US 12/418,071 Apr. 3, 2009 2010/0052112 Mar. 4, 2010 8,470,701 Jun. 25, 2013 216-06A US 12/522,582 Jul. 9, 2009 — — — — 38-04A1 US 12/564,566 Sep. 22, 2009 2010/0072577 Mar. 25, 2010 7,982,296 Jul. 19, 2011 71-07 US 12/669,287 Jan. 15, 2010 2011/0187798 Aug. 4, 2011 — — 60-09 US 12/778,588 May 12, 2010 2010/0317132 Dec. 16, 2010 — — 43-06A US 12/844,492 Jul. 27, 2010 2010/0289124 Nov. 18, 2010 8,039,847 Oct. 18, 2011 15-10 US 12/892,001 Sep. 28, 2010 2011/0230747 Sep. 22, 2011 8,666,471 Mar. 4, 2014 19-10 US 12/916,934 Nov. 1, 2010 2012/0105528 May 3, 2012 8,562,095 Oct. 22, 2013 3-10 US 12/947,120 Nov. 16,2010 2011/0170225 Jul. 14, 2011 — — 118-08 US 12/996,924 Dec. 8, 2010 2011/0147715 Jun. 23, 2011 8,946,683 Feb. 3, 2015 126-09 US 12/968,637 Dec. 15, 2010 2012/0157804 Jun. 21, 2012 — — 50-10 US 13/046,191 Mar. 11, 2011 2012/0165759 Jun. 28, 2012 — — 151-06A US 13/071,027 Mar. 24, 2011 2011/0171813 Jul. 14, 2011 — — 137-05A US 13/095,502 Apr. 27, 2011 — — — — 216-06B US 13/100,774 May 4, 2011 2011/0266561 Nov. 3, 2011 8,722,458 May 13, 2014 38-04A2 US 13/113,504 May 23, 2011 2011/0220890 Sep. 15, 2011 8,440,546 May 14, 2013 136-08 US 13/120,486 Aug. 4, 2011 2011/0277813 Nov. 17, 2011 8,679,888 Mar. 25, 2014 151-06B US 13/228,041 Sep. 8, 2011 2011/0316120 Dec. 29, 2011 — — 43-06B US 13/270,954 Oct. 11, 2011 2012/0083099 Apr. 5, 2012 8,394,706 Mar. 12, 2013 3-11 US 13/349,336 Jan. 12, 2012 2012/0261551 Oct. 18, 2012 — — 38-04E US 13/441,618 Apr. 6, 2012 2013/0100618 Apr. 25, 2013 8,754,396 Jun. 17, 2014 134-06B US 13/441,598 Apr. 6, 2012 2012/0327608 Dec. 27, 2012 8,729,524 May 20, 2014 28-11 US 13/472,165 May 15, 2012 2012/0320581 Dec. 20, 2012 — — 7-11 US 13/486,726 Jun. 1, 2012 2013/0072775 Mar. 21, 2013 8,934,965 Jan. 13, 2015 29-11 US 13/492,636 Jun. 8, 2012 2013/0041235 Feb. 14, 2013 — — 84-11 US 13/549,291 Jul. 13, 2012 2013/0036928 Feb. 14, 2013 — — 25-06A US 13/596,343 Aug. 28, 2012 2012/0321785 Dec. 20, 2012 8,367,035 Feb. 5, 2013 150-11 US 13/624,096 Sep. 21, 2012 2013/0140649 Jun. 6, 2013 — — 38-04A3 US 13/801,868 Mar. 13, 2013 2013/0320503 Dec. 5, 2013 8,664,699 Mar. 4, 2014 125-12 US 13/835,284 Mar. 15, 2013 2014/0220422 Aug. 7, 2014 — — 30-13 US 13/853,770 Mar. 29, 2013 2013/0333094 Dec. 19, 2013 — — 213-07A US 13/974,963 Aug. 23, 2013 2014/0140020 May 22, 2014 8,905,772 Dec. 9, 2014 19-10A US 14/033,765 Sep. 23, 2013 2014/0092158 Apr. 3, 2014 — — 15-10A US 14/140,299 Dec. 24, 2013 2014/0163390 Jun. 12, 2014 — — 38-04A4 US 14/155,010 Jan. 14, 2014 2014/0191236 Jul. 10, 2014 — — 136-08A US 14/173,525 Feb. 5, 2014 2014/0216524 Aug. 7, 2014 9,105,782 Aug. 11, 2015 216-06C US 14/209,481 Mar. 13, 2014 2014/0373898 Dec. 25, 2014 9,117,940 Aug. 25, 2015 134-06C US 14/220,910 Mar. 20, 2014 2014/0374872 Dec. 25, 2014 — — 38-04F US 14/220,923 Mar. 20, 2014 2015/0001462 Jan. 1, 2015 9,105,555 Aug. 11, 2015 151-06C US 14/246,962 Apr. 7, 2014 2014/0361409 Dec. 11, 2014 — — 62-13 US 14/250,671 Apr. 11, 2014 2014/0305900 Oct. 16, 2014 — — 56-13 US 14/251,259 Apr. 11, 2014 2014/0323968 Oct. 30, 2014 — — 60-09A US 12/778,588 Sep. 5, 2014 2015/0132873 May 14, 2015 — — 84-13 US 14/504,736 Oct. 2, 2014 2015/0141767 May 21, 2015 — — 213-07B US 14/521,319 Oct. 22, 2014 2015/0181700 Jun. 25, 2015 — — 7-11A US 14/532,687 Nov. 4, 2014 2015/0080695 Mar. 19, 2015 — — 2-14 US 14/599,290 Jan. 16, 2015 2015/0207012 Jul. 23, 2015 — — 71-07A US 12/669,287 Apr. 14, 2015 2015/0290938 Oct. 15, 2015 — — 213-07C US 12/398,811 May 7, 2015 2015/0237711 Aug. 20, 2015 — — 38-04G US 14/789,645 Jul. 1, 2015 — — — — 216-06D US 14/800,363 Jul. 15, 2015 — — — — 97-14 US 14/251,259 Aug. 4, 2015 — — — — 128-13 US 14/766,333 Aug. 6, 2015 — — — — 8-14 US 14/766,301 Aug. 6, 2015 — — — — 15-13 US 14/766,926 Aug. 10, 2015 — — — — 54-13 US 14/772,312 Sep. 2, 2015 — — — — 35-13 US 14/772,354 Sep. 2, 2015 — — — —

TABLE 1 Recommended daily intake and upper limits¹ for ingestion of Mo, P and SiO₂, average daily intake of Si from food^(2,3), and amounts in the blood and daily production of ammonia for adults⁴. Nutrients Mo P SiO₂ Recommended  45 mcg 700 mg 5-10 mg Daily Intakes Upper Limits 2000 mcg 4 g N/A Element Si (Source: food) Average Daily Intakes 20-50 mg Compound Ammonia (byproduct of Si₃N₄) Amount of Daily 17 g Production In the blood 0.7-2 mg/L *The amount of Si₃N₄ in a device is 264 mcg. The amount of ammonia generated by dissolution of the Si₃N₄ is 128.2 mcg. *Literature studies report a geographical correlation between the prevalence of Alzheimer's disease (AD) or various adverse effects on the central nervous system (CNS) in human brain and the concentration of aluminium ions (Al) in the brain from drinking water supplies^(5,6). The level of Al ions in the body can be significantly reduced by SiOH₄ (byproduct of dissolution of Si and SiO₂) by forming hydroxy-aluminosilicates (HAS)⁶. Studies also suggest that silicon-rich mineral waters can reduce the burden of aluminium in both Alzheimer's patients and control group⁷. 

We claim:
 1. An implantable and bioresorbable medical device comprising: a bioresorbable substrate; an electronic circuit supported by said bioresorbable substrate, wherein said electronic circuit comprises a membrane of silicon (Si) having a thickness less than or equal to 5 μm; an array of dissolvable electrodes, wherein said dissolvable electrodes are formed from said membrane of silicon; and wherein said electronic circuit is configured to conformally contact a biological tissue and electrically interface with the biological tissue during use.
 2. The implantable and bioresorbable device of claim 1, wherein said dissolvable electrodes are configured to undergo hydrolysis upon contact with a biofluid.
 3. The implantable and bioresorbable device of claim 1, wherein said array of dissolvable electrodes are a multiplexed array of dissolvable electrodes.
 4. The implantable and bioresorbable device of claim 3, further comprising an array of backplane transistors formed from said membrane of silicon in electrical contact with said array of dissolvable electrodes for high speed multiplexed addressing of said array of dissolvable electrodes.
 5. The implantable and bioresorbable device of claim 4, wherein said array of backplane transistors are MOSFETs.
 6. The implantable and bioresorbable device of claim 5, wherein said MOSFETs comprise a thin film of a metal, a gate dielectric and an interlayer dielectric.
 7. The implantable and bioresorbable device of claim 6, wherein: said metal comprises Molybdenum (Mo) having a thickness less than 500 nm; said gate dielectric comprises SiO₂ having a thickness less than 200 nm; said interlayer dielectric comprises a multilayer stack of SiO₂ with a thickness less than 400 nm, Si₃N₄ with a thickness less than 500 nm, and SiO₂ with a thickness less than 400 nm.
 8. The implantable and bioresorbable device of claim 4, further comprising for each electrode of the array of dissolvable electrodes: a buffer transistor electrically connected to said electrode of the array of dissolvable electrodes for buffering of a measured tissue potential; and a multiplexing transistor electrically connected to said electrode of the array of dissolvable electrodes for multiplexing of said array of dissolvable electrodes.
 9. The implantable and bioresorbable device of claim 8, further comprising a thin layer of metal electrically connected to said array of dissolvable electrodes to define column select lines.
 10. The implantable and bioresorbable device of claim 4, further comprising vertical interconnects to electrically connect said array of dissolvable electrodes to said array of backplane transistors, and said array of dissolvable electrodes are configured for physical contact with underlying tissue.
 11. The implantable and bioresorbable device of claim 10, wherein said vertical interconnects comprise vias.
 12. The implantable and bioresorbable device of claim 4, further comprising an encapsulation layer that covers said array of backplane transistors and said membrane of silicon.
 13. The implantable and bioresorbable device of claim 12, wherein said encapsulation layer comprises a bottom SiO₂ layer, a middle Si₃N₄ layer and a top SiO₂ layer.
 14. The implantable and bioresorbable device of claim 13, wherein said encapsulation layer has a thickness less than or equal to 2 μm.
 15. The implantable and bioresorbable device of claim 12, further comprising a plurality of passages through said encapsulation layer and in spatial alignment with an active region of each of said electrodes of said array of dissolvable electrodes.
 16. The implantable and bioresorbable device of claim 1, wherein said membrane of silicon is patterned to form a plurality of parallel silicon ribbons, the device further comprising: an encapsulation layer that covers a portion of said plurality of parallel silicon ribbons; and a plurality of passages formed through said encapsulation layer, wherein the passages are aligned with said plurality of parallel silicon ribbons to form an array of exposed silicon electrically interconnected to regions of encapsulated silicon ribbons.
 17. The implantable and bioresorbable device of claim 16, further comprising a plurality MOSFETs formed from said membrane of silicon, wherein said membrane of silicon serves as both an active semiconductor material and a tissue interface electrode.
 18. The implantable and bioresorbable device of claim 16, further comprising an active region at a distal end of said plurality of parallel silicon ribbons connected to external electrical connectors separated from said distal end by a longitudinal distance that is greater than or equal to 3 mm.
 19. The implantable and bioresorbable device of claim 1, wherein the membrane of silicon thickness, a dopant concentration in the membrane of silicon, or both the membrane of silicon thickness and the dopant concentration in the membrane of silicon are selected to provide for accurate measurement of a biological parameter over a device lifetime.
 20. The implantable and bioresorbable device of claim 19, wherein the membrane of silicon thickness and/or the dopant concentration in the membrane of silicon is selected to provide a device lifetime that is greater than or equal to 10 days.
 21. The implantable and bioresorbable device of claim 19, wherein the membrane of silicon thickness and/or the dopant concentration in the membrane of silicon is selected to provide a device lifetime that is less than or equal to 2 days.
 22. The implantable and bioresorbable device of claim 19, wherein said membrane of silicon has a thickness that decreases as a function of implant duration, wherein said device maintains functionality for a decrease in thickness of up to 70%.
 23. The implantable and bioresorbable device of claim 19, wherein device lifetime is increased with increasing dopant concentration in the membrane of silicon and/or increasing said membrane of silicon thickness.
 24. The implantable and bioresorbable device of claim 1, wherein said membrane of silicon is doped with a high concentration of dopant.
 25. The implantable and bioresorbable device of claim 24, wherein said high concentration of dopant is greater than or equal to 10¹⁸ cm⁻³ and less than or equal to 2×10²⁰ cm⁻³.
 26. The implantable and bioresorbable device of claim 24, wherein said dopant is selected from the group consisting of phosphorus and boron.
 27. The implantable and bioresorbable device of claim 1, further comprising an insulation layer and electrical interconnects that electrically connect said electrodes of said array of dissolvable electrodes, wherein said insulation layer electrically isolates the electrical interconnects from biofluids and biological tissue during use.
 28. The implantable and bioresorbable device of claim 27, wherein the insulation layer comprises a layer of SiO₂ having a thickness less than or equal to 200 nm.
 29. The implantable and bioresorbable device of claim 1, wherein said membrane of silicon further comprises terminal pads configured to electrically interface with a biological tissue.
 30. The implantable and bioresorbable device of claim 29, wherein said terminal pads are exposed Si of said membrane of Si.
 31. The implantable and bioresorbable device of claim 1, wherein: said membrane of silicon is doped with a concentration of dopant that is greater than or equal to 10¹⁸ cm⁻³ and less than or equal to 2×10²⁰ cm⁻³; and said membrane of silicon thickness and concentration of dopant are selected to provide a well-controlled dissolution rate of said membrane of silicon without cracking, fragmentation, flaking, or decrease in surface smoothness of the array of dissolvable electrodes over a time course of functional device lifetime.
 32. The implantable and bioresorbable device of claim 31, wherein said controlled dissolution of said array of dissolvable electrodes is characterized by one or more of no observable: cracks, flakes, particulates, or decrease in surface smoothness of said array of dissolvable electrodes.
 33. The implantable and bioresorbable device of claim 1, wherein said membrane of silicon has an average dissolution rate characterized by a decrease in Si membrane thickness that is greater than or equal to 5 nm/day and less than or equal to 15 nm/day.
 34. The implantable and bioresorbable device of claim 31, having a dissolution rate for components of the device that are not the membrane of silicon, including an insulating layer or said bioresorbable substrate, that is between 3 nm/day and 12 nm/day.
 35. The implantable and bioresorbable device of claim 1, having one or more material parameters selected to obtain a desired dissolution time of said device, the material parameters including one or more of silicon membrane thickness, silicon membrane doping level, or composition of polymer substrate.
 36. The implantable and bioresorbable device of claim 1, wherein during use the bioresorbable substrate, electronic circuit and array of dissolvable electrodes are configured for removal from the implant site by breakdown with exposure to a biological environment and biofluid such that there is no detectable long-term adverse immune response.
 37. The implantable and bioresorbable device of claim 1, wherein the bioresorbable substrate is configured to bend from a planar configuration to a curved configuration with a radius of curvature up to 3 mm without adverse degradation of device functionality.
 38. The implantable and bioresorbable device of claim 1, configured for spatio-temporal mapping of electrical activity for a biological tissue.
 39. The implantable and bioresorbable device of claim 38, configured for conformal contact with said biological tissue that is a cerebral cortex of brain.
 40. The implantable and bioresorbable device of claim 1, wherein the membrane of silicon comprises polycrystalline silicon.
 41. The implantable and bioresorbable device of claim 1, wherein the membrane of silicon comprises single-crystalline silicon.
 42. The implantable and bioresorbable device of claim 1, configured to detect electrical activity, application of an electric potential, or both of said biological tissue.
 43. A method of electrically interfacing with biological tissue, the method comprising the steps of: implanting at an implant site the implantable and bioresorbable medical device of claim 1 adjacent to a biological tissue; electrically interfacing the device with the biological tissue, wherein the interfacing is one or more of: electrically stimulating or electrically monitoring; maintaining device functionality over a device lifetime; and dissolving said device so that after said device lifetime no detectable device remains at said implant site. 